no DO ID for ribose_5_phosphate_isomerase_deficiency -> RPIA (SPAC144.12)
no DO ID for gracile_syndrome -> BCS1L (SPAC644.07)
no DO ID for peripheral_neuropathy_myopathy_hoarseness_and_hearing_loss -> MYH14 (SPCC645.05c)
no DO ID for infantile_liver_failure_syndrome_1 -> LARS (SPAC26F1.13c)
no DO ID for fumarase_deficiency -> FH (SPCC18.18c)
no DO ID for autoimmune_interstitial_lung_joint_and_kidney_disease -> COPA (SPBPJ4664.04)
no DO ID for myopathy_isolated_mitochondrial_autosomal_dominant -> CHCHD10 (SPAC6C3.02c)
no DO ID for hereditary_leiomyomatosis_and_renal_cell_cancer -> FH (SPCC18.18c)
no DO ID for alopecia_neurologic_defects_and_endocrinopathy_syndrome -> RBM28 (SPBC4F6.14)
no DO ID for combined_oxidative_phosphorylation_deficiency_21 -> TARS2 (SPAC24C9.09)
no DO ID for combined_oxidative_phosphorylation_deficiency_25 -> MARS2 (SPAC27E2.06c)
no DO ID for combined_oxidative_phosphorylation_deficiency_19 -> LYRM4 (SPBC13G1.06c)
no DO ID for cutaneous_telangiectasia_and_cancer_syndrome_familial -> ATR (SPBC216.05)
no DO ID for ataxia_telangiectasia_like_disorder_2 -> PCNA (SPBC16D10.09)
no DO ID for polymicrogyria_bilateral_temporooccipital -> FIG4 (SPAC1093.03)
no DO ID for spastic_ataxia_4_autosomal_recessive -> MTPAP (SPBC1685.06)
no DO ID for sensory_ataxic_neuropathy_dysarthria_and_ophthalmoparesis -> POLG (SPCC24B10.22)
no DO ID for myopathy_scapulohumeroperoneal -> ACTA1 (SPBC32H8.12c)
no DO ID for combined_d_2_and_l_2_hydroxyglutaric_aciduria -> SLC25A1 (SPAC19G12.05)
no DO ID for combined_malonic_and_methylmalonic_aciduria -> ACSF3 (SPCC1827.03c)
no DO ID for salla_disease -> SLC17A5 (SPAC1002.16c)
no DO ID for postaxial_acrofacial_dysostosis -> DHODH (SPAC57A10.12c)
no DO ID for congenital_disorder_of_glycosylation_type_iiq -> COG2 (SPBC36.08c)
no DO ID for spastic_paraplegia_72_autosomal_recessive -> REEP2 (SPBC30D10.09c)
no DO ID for miyoshi_muscular_dystrophy_1 -> DYSF (SPAC1296.04)
no DO ID for porphyria_acute_hepatic -> ALAD (SPAC1805.06c)
no DO ID for ataxia_telangiectasia_like_disorder_1 -> MRE11 (SPAC13C5.07)
no DO ID for combined_oxidative_phosphorylation_deficiency_12 -> EARS2 (SPAPB1A10.11c)
no DO ID for myopathy_distal_1 -> MYH7 (SPCC645.05c)
no DO ID for combined_oxidative_phosphorylation_deficiency_8 -> AARS2 (SPAC23C11.09)
no DO ID for tuberous_sclerosis_1_2 -> TSC1 (SPAC22F3.13)
no DO ID for combined_oxidative_phosphorylation_deficiency_3 -> TSFM (SPBC800.07c)
no DO ID for dihydrolipoamide_dehydrogenase_e3_deficiency -> DLD (SPAC1002.09c)
no DO ID for fish_eye_disease -> LCAT (SPBC776.14)
no DO ID for trimethylaminuria -> FMO3 (SPBP16F5.08c)
no DO ID for occipital_horn_syndrome -> ATP7A (SPBC29A3.01)
no DO ID for lathosterolosis -> SC5D (SPBC27B12.03c)
no DO ID for severe_combined_immunodeficiency_autosomal_recessive_t_cell_negative_b_cell_negative_nk_cell_negative_due_to_adenosine_deaminase_deficiency -> ADA (SPBC1198.02)
no DO ID for progressive_external_ophthalmoplegia_with_mitochondrial_dna_deletions_autosomal_recessive_1 -> POLG (SPCC24B10.22)
no DO ID for spinal_muscular_atrophy_lower_extremity_predominant_1_autosomal_dominant -> DYNC1H1 (SPAC1093.06c)
no DO ID for epilepsy_hearing_loss_and_mental_retardation_syndrome -> SPATA5 (SPBC56F2.07c)
no DO ID for coenzyme_q10_deficiency_primary_7 -> COQ4 (SPAC1687.12c)
no DO ID for mental_retardation_x_linked_102 -> DDX3X (SPCC1795.11)
no DO ID for combined_oxidative_phosphorylation_deficiency_10 -> MTO1 (SPBC30B4.06c)
no DO ID for kelley_seegmiller_syndrome -> HPRT1 (SPAC23C11.13c)
no DO ID for mental_retardation_x_linked_syndromic_turner_type -> HUWE1 (SPAC19D5.04)
no DO ID for you_hoover_fong_syndrome -> TELO2 (SPAC458.03)
no DO ID for cowden_syndrome_1 -> PTEN (SPBC609.02)
no DO ID for combined_oxidative_phosphorylation_deficiency_15 -> MTFMT (SPAC1805.09c)
no DO ID for deafness_x_linked_5 -> AIFM1 (SPAC26F1.14c)
no DO ID for homocystinuria_megaloblastic_anemia_cblg_complementation_type -> MTR (SPAC57A7.07c)
no DO ID for infantile_liver_failure_syndrome_2 -> NBAS (SPAC7D4.11c)
no DO ID for neurologic_endocrine_and_pancreatic_disease_multisystem_infantile_onset -> PTRH2 (SPAC19A8.14)
no DO ID for scapuloperoneal_myopathy_myh7_related -> MYH7 (SPCC645.05c)
no DO ID for leukoencephalopathy_with_brainstem_and_spinal_cord_involvement_and_lactate_elevation -> DARS2 (SPCC736.06)
no DO ID for epileptic_encephalopathy_early_infantile_50 -> CAD (SPBC215.08c)
no DO ID for lissencephaly_3 -> TUBA1A (SPBC16A3.15c)
no DO ID for liver_failure_infantile_transient -> TRMU (SPAC23H4.04)
no DO ID for focal_cortical_dysplasia_type_ii -> MTOR (SPBC30D10.10c)
no DO ID for n_acetylglutamate_synthase_deficiency -> NAGS (SPAC4G9.09c)
no DO ID for multisystemic_smooth_muscle_dysfunction_syndrome -> ACTA2 (SPBC32H8.12c)
no DO ID for phosphoribosylpyrophosphate_synthetase_superactivity -> PRPS1 (SPCC1620.06c)
no DO ID for spondylometaphyseal_dysplasia_with_cone_rod_dystrophy -> PCYT1A (SPCC1827.02c)
no DO ID for glycogen_storage_disease_xiii -> ENO3 (SPBPB21E7.01c)
no DO ID for catel_manzke_syndrome_2 -> TGDS (SPBPB2B2.11)
no DO ID for adenylosuccinase_deficiency -> ADSL (SPBC14F5.09c)
no DO ID for kanzaki_disease -> NAGA (SPAC869.07c)
no DO ID for spastic_ataxia_2_autosomal_recessive -> KIF1C (SPAC144.14)
no DO ID for thrombocytopenia_1 -> WAS (SPAC4F10.15c)
no DO ID for calcification_of_joints_and_arteries -> NT5E (SPBPB2B2.06c)
no DO ID for jalili_syndrome -> CNNM4 (SPCC4B3.03c)
no DO ID for muscular_dystrophy_limb_girdle_type_2b -> DYSF (SPAC1296.04)
no DO ID for mismatch_repair_cancer_syndrome -> PMS2 (SPAC19G12.02c)
no DO ID for iminoglycinuria -> SLC36A2 (SPAC3H1.09c)
no DO ID for congenital_disorder_of_glycosylation_type_ib -> MPI (SPBC2G2.16)
no DO ID for cholestasis_progressive_familial_intrahepatic_3_2 -> ABCB4 (SPCC663.03)
no DO ID for hypomyelination_with_brainstem_and_spinal_cord_involvement_and_leg_spasticity -> DARS (SPCC1223.07c)
no DO ID for nicolaides_baraitser_syndrome_2 -> SMARCA2 (SPCC1620.14c)
no DO ID for cholestasis_progressive_familial_intrahepatic_2_2 -> ABCB11 (SPCC663.03)
no DO ID for congenital_hemidysplasia_with_ichthyosiform_erythroderma_and_limb_defects -> NSDHL (SPBC3F6.02c)
no DO ID for short_stature_optic_nerve_atrophy_and_pelger_huet_anomaly -> NBAS (SPAC7D4.11c)
no DO ID for progressive_external_ophthalmoplegia_with_mitochondrial_dna_deletions_autosomal_recessive_2 -> RNASEH1 (SPBC336.06c)
no DO ID for combined_oxidative_phosphorylation_deficiency_14 -> FARS2 (SPCC736.03c)
no DO ID for hyperparathyroidism_2_with_jaw_tumors -> CDC73 (SPBC17G9.02c)
no DO ID for renal_tubular_acidosis_distal_autosomal_dominant -> SLC4A1 (SPBC543.05c)
no DO ID for hyperphenylalaninemia_bh4_deficient_b -> GCH1 (SPAC17A5.13)
no DO ID for interstitial_lung_and_liver_disease -> MARS (SPBC17A3.04c)
no DO ID for mismatch_repair_cancer_syndrome -> MLH1 (SPBC1703.04)
no DO ID for pyruvate_dehydrogenase_e1_beta_deficiency -> PDHB (SPBC30D10.13c)
no DO ID for majeed_syndrome -> LPIN2 (SPAC1952.13)
no DO ID for mitochondrial_phosphate_carrier_deficiency -> SLC25A3 (SPBC1703.13c)
no DO ID for phosphoglycerate_kinase_1_deficiency -> PGK1 (SPBC14F5.04c)
no DO ID for combined_oxidative_phosphorylation_deficiency_20 -> VARS2 (SPBC1709.02c)
no DO ID for combined_oxidative_phosphorylation_deficiency_11 -> RMND1 (SPCC16C4.01)
no DO ID for porphyria_congenital_erythropoietic -> UROS (SPAC31G5.08)
no DO ID for combined_oxidative_phosphorylation_deficiency_24 -> NARS2 (SPBC1198.10c)
no DO ID for combined_oxidative_phosphorylation_deficiency_6 -> AIFM1 (SPAC26F1.14c)
no DO ID for microcephaly_capillary_malformation_syndrome -> STAMBP (SPAC19B12.10)
no DO ID for neutropenia_severe_congenital_x_linked -> WAS (SPAC4F10.15c)
no DO ID for mitochondrial_pyruvate_carrier_deficiency -> MPC1 (SPCC1235.11)
no DO ID for short_stature_developmental_delay_and_congenital_heart_defects -> TKT (SPBC2G5.05)
no DO ID for ruijs_aalfs_syndrome -> SPRTN (SPBC19G7.04)
no DO ID for microcephaly_epilepsy_and_diabetes_syndrome -> IER3IP1 (SPAC19A8.09)
no DO ID for smith_kingsmore_syndrome -> MTOR (SPBC30D10.10c)
no DO ID for dystonia_4_torsion_autosomal_dominant -> TUBB4A (SPBC26H8.07c)
no DO ID for bisphosphoglycerate_mutase_deficiency -> BPGM (SPAC26F1.06)
no DO ID for dent_disease_2 -> OCRL (SPBC577.13)
no DO ID for codas_syndrome -> LONP1 (SPAC22F3.06c)
no DO ID for microcephaly_amish_type -> SLC25A19 (SPBC1604.04)
no DO ID for pierpont_syndrome -> TBL1XR1 (SPCC1235.09)
no DO ID for epilepsy_familial_focal_with_variable_foci_1_2 -> DEPDC5 (SPBC26H8.04c)
no DO ID for renal_tubular_acidosis_proximal_with_ocular_abnormalities_and_mental_retardation -> SLC4A4 (SPBC543.05c)
no DO ID for encephalopathy_progressive_early_onset_with_brain_atrophy_and_thin_corpus_callosum -> TBCD (SPBC11C11.04c)
no DO ID for microcephaly_progressive_with_seizures_and_cerebral_and_cerebellar_atrophy -> QARS (SPBC342.02)
no DO ID for lipid_storage_myopathy_due_to_flavin_adenine_dinucleotide_synthetase_deficiency -> FLAD1 (SPCC1235.04c)
no DO ID for lethal_arthrogryposis_with_anterior_horn_cell_disease -> GLE1 (SPBC31E1.05)
no DO ID for combined_oxidative_phosphorylation_deficiency_17 -> ELAC2 (SPBC3D6.03c)
no DO ID for coenzyme_q10_deficiency_primary_4 -> COQ8A (SPBC2D10.18)
no DO ID for bone_marrow_failure_syndrome_1 -> SRP72 (SPCC320.10)
no DO ID for encephalopathy_due_to_defective_mitochondrial_and_peroxisomal_fission_1 -> DNM1L (SPAC767.01c)
no DO ID for radiohumeral_fusions_with_other_skeletal_and_craniofacial_anomalies -> CYP26B1 (SPAC19A8.04)
no DO ID for mental_retardation_autosomal_recessive_53 -> PIGG (SPAC13G6.03)
no DO ID for osteochondrodysplasia_complex_lethal_symoens_barnes_gistelinck_type -> TAPT1 (SPBC13G1.05)
no DO ID for combined_oxidative_phosphorylation_deficiency_23 -> GTPBP3 (SPAC222.05c)
no DO ID for congenital_disorder_of_glycosylation_type_iim -> SLC35A2 (SPCC1795.03)
no DO ID for progressive_external_ophthalmoplegia_with_mitochondrial_dna_deletions_autosomal_dominant_6_2 -> DNA2 (SPBC16D10.04c)
no DO ID for homocystinuria_megaloblastic_anemia_cble_complementation_type -> MTRR (SPBC12C2.03c)
no DO ID for spinal_muscular_atrophy_jokela_type -> CHCHD10 (SPAC6C3.02c)
no DO ID for autoinflammation_antibody_deficiency_and_immune_dysregulation_plcg2_associated -> PLCG2 (SPAC22F8.11)
no DO ID for mental_retardation_x_linked_syndromic_33_2 -> TAF1 (SPAC2G11.14)
no DO ID for coloboma_congenital_heart_disease_ichthyosiform_dermatosis_mental_retardation_and_ear_anomalies_syndrome -> PIGL (SPAPB2B4.01c)
no DO ID for hyperphenylalaninemia_bh4_deficient_d -> PCBD1 (SPAC27D7.04)
no DO ID for mandibuloacral_dysplasia_with_type_b_lipodystrophy -> ZMPSTE24 (SPAC3H1.05)
no DO ID for renal_tubular_acidosis_distal_with_hemolytic_anemia -> SLC4A1 (SPBC543.05c)
no DO ID for aicar_transformylase_imp_cyclohydrolase_deficiency -> ATIC (SPCPB16A4.03c)
no DO ID for coenzyme_q10_deficiency_primary_6 -> COQ6 (SPBC146.12)
no DO ID for cerebral_arteriopathy_autosomal_recessive_with_subcortical_infarcts_and_leukoencephalopathy -> HTRA1 (SPAC23G3.12c)
no DO ID for linear_skin_defects_with_multiple_congenital_anomalies_1 -> HCCS (SPAC24C9.02c)
no DO ID for myopathy_mitochondrial_progressive_with_congenital_cataract_hearing_loss_and_developmental_delay -> GFER (SPBC146.04)
no DO ID for boucher_neuhauser_syndrome_2 -> PNPLA6 (SPCC4B3.04c)
no DO ID for cholestasis_benign_recurrent_intrahepatic_2 -> ABCB11 (SPCC663.03)
no DO ID for combined_oxidative_phosphorylation_deficiency_1 -> GFM1 (SPBC1306.01c)
no DO ID for combined_oxidative_phosphorylation_deficiency_26 -> TRMT5 (SPAPB18E9.01)
no DO ID for ataxia_oculomotor_apraxia_4 -> PNKP (SPAC23C11.04c)
no DO ID for mental_retardation_x_linked_syndromic_nascimento_type -> UBE2A (SPAC18B11.07c)
no DO ID for polyglucosan_body_myopathy_2 -> GYG1 (SPAC5H10.12c)
no DO ID for combined_oxidative_phosphorylation_deficiency_4 -> TUFM (SPBC9B6.04c)
no DO ID for hyperuricemia_pulmonary_hypertension_renal_failure_and_alkalosis_syndrome -> SARS2 (SPAC25B8.06c)
no DO ID for microcephaly_postnatal_progressive_with_seizures_and_brain_atrophy -> MED17 (SPBC31F10.04c)
no DO ID for spinal_muscular_atrophy_x_linked_2 -> UBA1 (SPBC1604.21c)
no DO ID for asparagine_synthetase_deficiency -> ASNS (SPBC119.10)
no DO ID for coenzyme_q10_deficiency_primary_2 -> PDSS1 (SPBPJ4664.01)
no DO ID for anemia_sideroblastic_3_pyridoxine_refractory -> GLRX5 (SPAPB2B4.02)
no DO ID for striatonigral_degeneration_childhood_onset -> VAC14 (SPBC25H2.03)
no DO ID for ohdo_syndrome_x_linked -> MED12 (SPAC688.08)
no DO ID for mental_retardation_autosomal_recessive_40 -> TAF2 (SPAC3A12.05c)
no DO ID for asplenia_isolated_congenital -> RPSA (SPBC685.06)
no DO ID for combined_oxidative_phosphorylation_deficiency_9 -> MRPL3 (SPAC644.17c)
no DO ID for pulmonary_venoocclusive_disease_2_autosomal_recessive -> EIF2AK4 (SPBC36B7.09)
no DO ID for congenital_cataracts_hearing_loss_and_neurodegeneration -> SLC33A1 (SPBC21B10.09)
no DO ID for erythrocyte_lactate_transporter_defect -> SLC16A1 (SPAC2G11.13)
no DO ID for mental_retardation_autosomal_recessive_49 -> GPT2 (SPBC582.08)
no DO ID for immunodeficiency_23 -> PGM3 (SPAC13C5.05c)
no DO ID for lipoyltransferase_1_deficiency -> LIPT1 (SPBC17A3.09c)
no DO ID for neutropenia_severe_congenital_5_autosomal_recessive -> VPS45 (SPAC2G11.03c)
no DO ID for epilepsy_progressive_myoclonic_6_2 -> GOSR2 (SPAP14E8.03)
no DO ID for spastic_ataxia_5_autosomal_recessive -> AFG3L2 (SPBC543.09)
no DO ID for mental_retardation_autosomal_recessive_39 -> TTI2 (SPBC1604.17c)
no DO ID for oliver_mcfarlane_syndrome -> PNPLA6 (SPCC4B3.04c)
no DO ID for trichohepatoenteric_syndrome_1 -> TTC37 (SPCC1919.05)
no DO ID for congenital_disorder_of_glycosylation_type_ij -> DPAGT1 (SPBC15D4.04)
no DO ID for thiamine_metabolism_dysfunction_syndrome_4 -> SLC25A19 (SPBC1604.04)
no DO ID for congenital_disorder_of_glycosylation_type_ih -> ALG8 (SPAC17C9.07)
no DO ID for mental_retardation_autosomal_recessive_36 -> ADAT3 (SPAP27G11.04c)
no DO ID for hypertriglyceridemia_transient_infantile -> GPD1 (SPBC215.05)
no DO ID for congenital_disorder_of_glycosylation_type_id -> ALG3 (SPAC7D4.06c)
no DO ID for hyperglycinemia_lactic_acidosis_and_seizures -> LIAS (SPBC8D2.15)
no DO ID for congenital_disorder_of_glycosylation_type_ie -> DPM1 (SPAC31G5.16c)
no DO ID for cerebellofaciodental_syndrome -> BRF1 (SPBC13E7.10c)
no DO ID for craniolenticulosutural_dysplasia -> SEC23A (SPBC776.04)
no DO ID for myopathy_centronuclear_2 -> BIN1 (SPBC21D10.12)
no DO ID for immunodeficiency_8 -> CORO1A (SPAC23C4.02)
no DO ID for cerebrocostomandibular_syndrome -> SNRPB (SPAC26A3.08)
no DO ID for immunodeficiency_34 -> CYBB (SPBC1683.09c)
no DO ID for 3_hydroxyisobutyryl_coa_hydrolase_deficiency -> HIBCH (SPBC2D10.09)
no DO ID for charcot_marie_tooth_disease_axonal_autosomal_dominant_type_2a2a -> MFN2 (SPBC1706.03)
no DO ID for epiphyseal_dysplasia_multiple_4 -> SLC26A2 (SPBC3H7.02)
no DO ID for spinal_muscular_atrophy_type_iii -> SMN1 (SPAC2G11.08c)
no DO ID for hyperinsulinemic_hypoglycemia_familial_6 -> GLUD1 (SPCC132.04c)
no DO ID for focal_cortical_dysplasia_type_ii -> TSC1 (SPAC22F3.13)
no DO ID for severe_combined_immunodeficiency_with_microcephaly_growth_retardation_and_sensitivity_to_ionizing_radiation -> NHEJ1 (SPCC24B10.14c)
no DO ID for glutamine_deficiency_congenital -> GLUL (SPAC23H4.06)
no DO ID for hemolytic_anemia_nonspherocytic_due_to_glucose_phosphate_isomerase_deficiency -> GPI (SPBC1604.05)
no DO ID for 17_beta_hydroxysteroid_dehydrogenase_iii_deficiency -> HSD17B3 (SPAC4G9.15)
no DO ID for spinal_muscular_atrophy_late_onset_finkel_type -> VAPB (SPBC16G5.05c)
no DO ID for schindler_disease_type_i -> NAGA (SPAC869.07c)
no DO ID for myopathy_lactic_acidosis_and_sideroblastic_anemia_1 -> PUS1 (SPCC16C4.06c)
no DO ID for congenital_disorder_of_glycosylation_type_iij -> COG4 (SPCC338.13)
no DO ID for congenital_disorder_of_glycosylation_type_iik -> TMEM165 (SPAC17G8.08c)
no DO ID for congenital_disorder_of_glycosylation_type_iic -> SLC35C1 (SPAC22F8.04)
no DO ID for congenital_disorder_of_glycosylation_type_ip -> ALG11 (SPCC330.08)
no DO ID for gamma_glutamylcysteine_synthetase_deficiency_hemolytic_anemia_due_to -> GCLC (SPAC22F3.10c)
no DO ID for spondylometaphyseal_dysplasia_megarbane_dagher_melki_type -> PAM16 (SPBC713.10)
no DO ID for hyperinsulinemic_hypoglycemia_familial_3_2 -> GCK (SPAC4F8.07c)
no DO ID for glycogen_storage_disease_x -> PGAM2 (SPAC26F1.06)
no DO ID for rh_null_regulator_type -> RHAG (SPAC2E1P3.02c)
no DO ID for anemia_congenital_dyserythropoietic_type_ii -> SEC23B (SPBC776.04)
no DO ID for arthrogryposis_distal_type_2a -> MYH3 (SPCC645.05c)
no DO ID for arthrogryposis_distal_type_5 -> MYH3 (SPCC645.05c)
no DO ID for arthrogryposis_distal_type_7 -> MYH8 (SPCC645.05c)
no DO ID for arthrogryposis_distal_type_8 -> MYH3 (SPCC645.05c)
no DO ID for congenital_disorder_of_glycosylation_type_ic -> ALG6 (SPBC342.01c)
no DO ID for congenital_disorder_of_glycosylation_type_iib -> MOGS (SPAC6G10.09)
no DO ID for congenital_disorder_of_glycosylation_type_iil_2 -> COG6 (SPBC776.10c)
no DO ID for congenital_disorder_of_glycosylation_type_im -> DOLK (SPCC63.10c)
no DO ID for congenital_disorder_of_glycosylation_type_io -> DPM3 (SPBC1677.02)
no DO ID for folate_malabsorption_hereditary -> SLC46A1 (SPAC14C4.07)
no DO ID for heart_defects_congenital_and_other_congenital_anomalies -> GATA6 (SPCC1902.01)
no DO ID for hemolytic_anemia_nonspherocytic_due_to_hexokinase_deficiency -> HK1 (SPAC4F8.07c)
no DO ID for optic_atrophy_3_autosomal_dominant -> OPA3 (SPBC1703.11)
no DO ID for pseudohypoaldosteronism_type_iie_2 -> CUL3 (SPAC24H6.03)
no DO ID for robin_sequence_with_cleft_mandible_and_limb_anomalies -> EIF4A3 (SPAC1F5.10)
no DO ID for spinal_muscular_atrophy_distal_x_linked_3 -> ATP7A (SPBC29A3.01)
no DO ID for cataracts_growth_hormone_deficiency_sensory_neuropathy_sensorineural_hearing_loss_and_skeletal_dysplasia -> IARS2 (SPCC18B5.08c)
no DO ID for combined_oxidative_phosphorylation_deficiency_34 -> MRPS7 (SPAC16E8.10c)
no DO ID for glutathione_synthetase_deficiency -> GSS (SPAC3F10.04)
no DO ID for galactosialidosis -> CTSA (SPAC19G12.10c)
no DO ID for congenital_disorder_of_glycosylation_type_ia_2 -> PMM2 (SPAC1556.07)
no DO ID for 3_hydroxy_3_methylglutaryl_coa_synthase_2_deficiency_2 -> HMGCS2 (SPAC4F8.14c)
no DO ID for familial_adenomatous_polyposis_2 -> MUTYH (SPAC26A3.02)
no DO ID for hyper_igd_syndrome -> MVK (SPAC13G6.11c)
no DO ID for congenital_disorder_of_glycosylation_type_ik -> ALG1 (SPAC23C4.14)
no DO ID for melanocytic_nevus_syndrome_congenital -> NRAS (SPAC17H9.09c)
no DO ID for takenouchi_kosaki_syndrome -> CDC42 (SPAC110.03)
no DO ID for aplasia_cutis_congenita_nonsyndromic -> BMS1 (SPBC31E1.06)
no DO ID for congenital_disorder_of_glycosylation_type_ir -> DDOST (SPCC338.15)
no DO ID for hyperprolinemia_type_i -> PRODH (SPCC70.03c)
no DO ID for homocystinuria_due_to_cystathionine_beta_synthase_deficiency -> CBS (SPBC36.04)
no DO ID for spinocerebellar_ataxia_autosomal_recessive_with_axonal_neuropathy_2 -> TDP1 (SPCP31B10.05)
no DO ID for combined_oxidative_phosphorylation_deficiency_28 -> SLC25A26 (SPBC1271.11)
no DO ID for gaba_transaminase_deficiency -> ABAT (SPAC19D5.07)
no DO ID for even_plus_syndrome -> HSPA9 (SPAC664.11)
no DO ID for peho_syndrome -> ZNHIT3 (SPAC4F10.19c)
no DO ID for cryohydrocytosis -> SLC4A1 (SPBC543.05c)
no DO ID for myopathy_centronuclear_x_linked -> MTM1 (SPAC19A8.03)
no DO ID for anemia_hypochromic_microcytic_with_iron_overload_1 -> SLC11A2 (SPAC27F1.08)
no DO ID for combined_oxidative_phosphorylation_deficiency_31 -> MIPEP (SPAC1F3.10c)
no DO ID for pyogenic_sterile_arthritis_pyoderma_gangrenosum_and_acne -> PSTPIP1 (SPBC11C11.02)
no DO ID for microcephaly_congenital_cataract_and_psoriasiform_dermatitis -> MSMO1 (SPAC630.08c)
no DO ID for gallbladder_disease_1 -> ABCB4 (SPCC663.03)
no DO ID for congenital_disorder_of_glycosylation_type_iip -> TMEM199 (SPCC757.10)
no DO ID for multiple_mitochondrial_dysfunctions_syndrome_2_with_hyperglycinemia -> BOLA3 (SPCC4B3.11c)
no DO ID for hypoinsulinemic_hypoglycemia_with_hemihypertrophy -> AKT2 (SPCC24B10.07)
no DO ID for overhydrated_hereditary_stomatocytosis -> RHAG (SPAC2E1P3.02c)
no DO ID for myopathy_mitochondrial_and_ataxia -> MSTO1 (SPAC30C2.06c)
no DO ID for congenital_disorder_of_glycosylation_type_ig -> ALG12 (SPBC1734.12c)
no DO ID for myopathy_distal_5 -> ADSSL1 (SPAC144.03)
no DO ID for myopathy_proximal_and_ophthalmoplegia -> MYH2 (SPCC645.05c)
no DO ID for infantile_sialic_acid_storage_disease -> SLC17A5 (SPAC1002.16c)
no DO ID for pyridoxamine_5_prime_phosphate_oxidase_deficiency -> PNPO (SPAC1093.02)
no DO ID for hyperprolinemia_type_ii -> ALDH4A1 (SPBC24C6.04)
no DO ID for homocystinuria_due_to_deficiency_of_n_methylenetetrahydrofolate_reductase_activity -> MTHFR (SPAC343.10)
no DO ID for 3_methylglutaconic_aciduria_type_viii -> HTRA2 (SPAC23G3.12c)
no DO ID for methionine_adenosyltransferase_i_iii_deficiency -> MAT1A (SPBC14F5.05c)
no DO ID for macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss -> MYH9 (SPCC645.05c)
no DO ID for congenital_disorder_of_glycosylation_type_iu -> DPM2 (SPBC21B10.11)
no DO ID for spondyloepimetaphyseal_dysplasia_with_joint_laxity_type_2 -> KIF22 (SPBC1604.20c)
no DO ID for rhabdoid_tumor_predisposition_syndrome_1 -> SMARCB1 (SPCC16A11.14)
no DO ID for chondrodysplasia_with_platyspondyly_distinctive_brachydactyly_hydrocephaly_and_microphthalmia -> HDAC6 (SPBC800.03)
no DO ID for retinal_dystrophy_juvenile_cataracts_and_short_stature_syndrome -> RDH11 (SPCC736.13)
no DO ID for arthrogryposis_mental_retardation_and_seizures -> SLC35A3 (SPCC1795.03)
no DO ID for polyendocrine_polyneuropathy_syndrome -> DMXL2 (SPBC1105.10)
no DO ID for meckel_syndrome_12 -> KIF14 (SPAC144.14)
no DO ID for diarrhea_7 -> DGAT1 (SPCP1E11.05c)
no DO ID for nijmegen_breakage_syndrome_like_disorder -> RAD50 (SPAC1556.01c)
no DO ID for microphthalmia_syndromic_1 -> NAA10 (SPAC15E1.08)
no DO ID for hypercholesterolemia_autosomal_dominant_3 -> PCSK9 (SPAC1006.01)
no DO ID for glomuvenous_malformations -> GLMN (SPAC15F9.01c)
no DO ID for reynolds_syndrome -> LBR (SPBC16G5.18)
no DO ID for seizures_cortical_blindness_and_microcephaly_syndrome -> DIAPH1 (SPAC1F5.04c)
no DO ID for premature_chromatid_separation_trait -> BUB1B (SPCC1322.12c)
no DO ID for hydrops_lactic_acidosis_and_sideroblastic_anemia -> LARS2 (SPAC4G8.09)
no DO ID for inosine_triphosphatase_deficiency -> ITPA (SPCC830.10)
no DO ID for perrault_syndrome_2 -> HARS2 (SPBC2G2.12)
no DO ID for zttk_syndrome -> SON (SPCC1442.13c)
no DO ID for floating_harbor_syndrome -> SRCAP (SPAC11E3.01c)
no DO ID for pyruvate_dehydrogenase_phosphatase_deficiency -> PDP1 (SPAC10F6.17c)
no DO ID for congenital_disorder_of_glycosylation_type_ix -> STT3B (SPBC1271.02)
no DO ID for buschke_ollendorff_syndrome -> LEMD3 (SPAC14C4.05c)
no DO ID for facial_dysmorphism_immunodeficiency_livedo_and_short_stature -> POLE (SPBC25H2.13c)
no DO ID for 5_oxoprolinase_deficiency -> OPLAH (SPAC11D3.15)
no DO ID for genitopatellar_syndrome -> KAT6B (SPAC17G8.13c)
no DO ID for hyperoxaluria_primary_type_ii -> GRHPR (SPBC1773.17c)
no DO ID for adermatoglyphia -> SMARCAD1 (SPAC25A8.01c)
no DO ID for witteveen_kolk_syndrome -> SIN3A (SPBC1734.16c)
no DO ID for diaphyseal_medullary_stenosis_with_malignant_fibrous_histiocytoma -> MTAP (SPAC16C9.02c)
no DO ID for cerebrooculofacioskeletal_syndrome_2 -> ERCC2 (SPAC1D4.12)
no DO ID for tuberous_sclerosis_2 -> TSC2 (SPAC18B11.11)
no DO ID for pyruvate_dehydrogenase_e3_binding_protein_deficiency -> PDHX (SPCC1259.09c)
no DO ID for transaldolase_deficiency -> TALDO1 (SPCC1020.06c)
no DO ID for mandibular_hypoplasia_deafness_progeroid_features_and_lipodystrophy_syndrome -> POLD1 (SPBC336.04)
no DO ID for pyruvate_dehydrogenase_e2_deficiency -> DLAT (SPCC794.07)
no DO ID for congenital_cataracts_facial_dysmorphism_and_neuropathy -> CTDP1 (SPAC19B12.05c)
no DO ID for wrinkly_skin_syndrome -> ATP6V0A2 (SPAC16E8.07c)
no DO ID for colorectal_cancer_12 -> POLE (SPBC25H2.13c)
no DO ID for tarp_syndrome -> RBM10 (SPAC57A7.13)
no DO ID for alazami_syndrome -> LARP7 (SPAC17G6.17)
no DO ID for glycosylphosphatidylinositol_deficiency -> PIGM (SPBC13E7.05)
no DO ID for pheochromocytoma -> SDHB (SPAC140.01)
no DO ID for pulmonary_fibrosis_and_or_bone_marrow_failure_telomere_related_1 -> TERT (SPBC29A3.14c)
no DO ID for paraganglioma_and_gastric_stromal_sarcoma -> SDHD (SPBP23A10.16)
no DO ID for immunodeficiency_x_linked_with_magnesium_defect_epstein_barr_virus_infection_and_neoplasia -> MAGT1 (SPAPB17E12.11)
no DO ID for paraganglioma_and_gastric_stromal_sarcoma -> SDHB (SPAC140.01)
no DO ID for cardioencephalomyopathy_fatal_infantile_due_to_cytochrome_c_oxidase_deficiency_3 -> COA5 (SPBC16A3.16)
no DO ID for atrial_fibrillation_familial_18 -> MYL4 (SPAP8A3.08)
no DO ID for diamond_blackfan_anemia_14_with_mandibulofacial_dysostosis -> TSR2 (SPBC409.15)
no DO ID for bone_mineral_density_quantitative_trait_locus_18 -> PLS3 (SPBC1778.06c)
no DO ID for keratosis_linearis_with_ichthyosis_congenita_and_sclerosing_keratoderma -> POMP (SPCC14G10.03c)
no DO ID for cerebellar_ataxia_mental_retardation_and_dysequilibrium_syndrome_4 -> ATP8A2 (SPBC887.12)
no DO ID for pigmentary_disorder_reticulate_with_systemic_manifestations_x_linked -> POLA1 (SPAC3H5.06c)
no DO ID for combined_oxidative_phosphorylation_deficiency_7 -> C12orf65 (SPBC1105.18c)
no DO ID for epileptic_encephalopathy_early_infantile_35 -> ITPA (SPCC830.10)
no DO ID for peroxisome_biogenesis_disorder_10b -> PEX3 (SPAC29A4.14c)
no DO ID for prostate_cancer_hereditary_2 -> ELAC2 (SPBC3D6.03c)
no DO ID for familial_adenomatous_polyposis_4 -> MSH3 (SPAC8F11.03)
no DO ID for combined_oxidative_phosphorylation_deficiency_22 -> ATP5F1A (SPAC14C4.14)
no DO ID for coenzyme_q10_deficiency_primary_5 -> COQ9 (SPAC19G12.11)
no DO ID for combined_oxidative_phosphorylation_deficiency_18 -> SFXN4 (SPAC17G6.15c)
no DO ID for epileptic_encephalopathy_early_infantile_40 -> GUF1 (SPAC1B3.04c)
no DO ID for spinocerebellar_ataxia_autosomal_recessive_24_2 -> UBA5 (SPAC1A6.10)
no DO ID for nephrolithiasis_calcium_oxalate -> SLC26A1 (SPBC3H7.02)
no DO ID for familial_adenomatous_polyposis_3 -> NTHL1 (SPAC30D11.07)
no DO ID for atrial_fibrillation_familial_15 -> NUP155 (SPBP35G2.06c)
no DO ID for meier_gorlin_syndrome_5 -> CDC6 (SPBC14C8.07c)
no DO ID for ichthyosis_spastic_quadriplegia_and_mental_retardation -> ELOVL4 (SPAC1639.01c)
no DO ID for kohlschutter_tonz_syndrome_2 -> ROGDI (SPBC3H7.12)
no DO ID for encephalopathy_progressive_with_or_without_lipodystrophy -> BSCL2 (SPAC3A11.04)
no DO ID for combined_oxidative_phosphorylation_deficiency_2 -> MRPS16 (SPBC354.06)
no DO ID for spasticity_childhood_onset_with_hyperglycinemia -> GLRX5 (SPAPB2B4.02)
no DO ID for congenital_disorder_of_glycosylation_type_iih -> COG8 (SPBC11B10.03)
no DO ID for deafness_congenital_with_onychodystrophy_autosomal_dominant -> ATP6V1B2 (SPAC637.05c)
no DO ID for optic_atrophy_9 -> ACO2 (SPAC24C9.06c)
no DO ID for microcephaly_18_primary_autosomal_dominant -> WDFY3 (SPBC28E12.06c)
no DO ID for optic_atrophy_11 -> YME1L1 (SPCC965.04c)
no DO ID for immunodeficiency_24 -> CTPS1 (SPAC10F6.03c)
no DO ID for mismatch_repair_cancer_syndrome -> MSH6 (SPCC285.16c)
no DO ID for cockayne_syndrome_b -> ERCC6 (SPCP25A2.02c)
no DO ID for microcephaly_seizures_and_developmental_delay -> PNKP (SPAC23C11.04c)
no DO ID for mismatch_repair_cancer_syndrome -> MSH2 (SPBC19G7.01c)
no DO ID for myopathy_distal_with_anterior_tibial_onset -> DYSF (SPAC1296.04)
no DO ID for protoporphyria_erythropoietic_x_linked -> ALAS2 (SPAC2F3.09)
no DO ID for immunodeficiency_due_to_defect_in_mapbp_interacting_protein -> LAMTOR2 (SPBC1778.05c)
no DO ID for cortical_dysplasia_complex_with_other_brain_malformations_8 -> TUBA8 (SPBC16A3.15c)
no DO ID for glutathione_synthetase_deficiency_of_erythrocytes_hemolytic_anemia_due_to -> GSS (SPAC3F10.04)
no DO ID for spastic_ataxia_3_autosomal_recessive -> MARS2 (SPAC27E2.06c)
no DO ID for myopathy_with_lactic_acidosis_hereditary -> ISCU (SPAC227.13c)
no DO ID for congenital_disorder_of_glycosylation_type_iaa -> NUS1 (SPBC2A9.06c)
no DO ID for cataract_47 -> SLC16A12 (SPAC2G11.13)
no DO ID for nephrotic_syndrome_type_13_2 -> NUP205 (SPCC290.03c)
no DO ID for aicardi_goutieres_syndrome_2 -> RNASEH2B (SPBC1347.08c)
no DO ID for kaufman_oculocerebrofacial_syndrome -> UBE3B (SPAC167.07c)
no DO ID for treacher_collins_syndrome_3 -> POLR1C (SPBC1289.07c)
no DO ID for cornelia_de_lange_syndrome_1 -> NIPBL (SPAC31A2.05c)
no DO ID for aortic_aneurysm_familial_thoracic_4 -> MYH11 (SPCC645.05c)
no DO ID for amyotrophic_lateral_sclerosis_14_with_or_without_frontotemporal_dementia_2 -> VCP (SPAC1565.08)
no DO ID for paragangliomas_5 -> SDHA (SPAC1556.02c)
no DO ID for aortic_aneurysm_familial_thoracic_6 -> ACTA2 (SPBC32H8.12c)
no DO ID for hyperphosphatasia_with_mental_retardation_syndrome_2 -> PIGO (SPBC27B12.06)
no DO ID for dystonia_childhood_onset_with_optic_atrophy_and_basal_ganglia_abnormalities -> MECR (SPAC26F1.04c)
no DO ID for epileptic_encephalopathy_early_infantile_31 -> DNM1 (SPAC767.01c)
no DO ID for atelosteogenesis_type_ii -> SLC26A2 (SPBC3H7.02)
no DO ID for goiter_multinodular_1_with_or_without_sertoli_leydig_cell_tumors -> DICER1 (SPCC188.13c)
no DO ID for paragangliomas_4 -> SDHB (SPAC140.01)
no DO ID for epileptic_encephalopathy_early_infantile_33 -> EEF1A2 (SPAC23A1.10)
no DO ID for aicardi_goutieres_syndrome_6 -> ADAR (SPBC16A3.06)
no DO ID for peroxisome_biogenesis_disorder_9b -> PEX7 (SPAC17D4.01)
no DO ID for li_fraumeni_syndrome_2 -> CHEK2 (SPCC18B5.11c)
no DO ID for neurodevelopmental_disorder_with_involuntary_movements -> GNAO1 (SPBC24C6.06)
no DO ID for myopathy_myosin_storage_autosomal_recessive -> MYH7 (SPCC645.05c)
no DO ID for hyperphosphatasia_with_mental_retardation_syndrome_1 -> PIGV (SPAC18B11.05)
no DO ID for mental_retardation_autosomal_recessive_15 -> MAN1B1 (SPAC2E1P5.01c)
no DO ID for porokeratosis_3_multiple_types -> MVK (SPAC13G6.11c)
no DO ID for meier_gorlin_syndrome_2 -> ORC4 (SPBP23A10.13)
no DO ID for combined_oxidative_phosphorylation_deficiency_16 -> MRPL44 (SPBC3B9.14c)
no DO ID for auriculocondylar_syndrome_2 -> PLCB4 (SPAC22F8.11)
no DO ID for cardiofaciocutaneous_syndrome_2 -> KRAS (SPAC17H9.09c)
no DO ID for alazami_yuan_syndrome -> TAF6 (SPCC16C4.18c)
no DO ID for perrault_syndrome_4 -> LARS2 (SPAC4G8.09)
no DO ID for sucrase_isomaltase_deficiency_congenital -> SI (SPAC30D11.01c)
no DO ID for melanosis_neurocutaneous -> NRAS (SPAC17H9.09c)
no DO ID for moyamoya_disease_5 -> ACTA2 (SPBC32H8.12c)
no DO ID for aicardi_goutieres_syndrome_3 -> RNASEH2C (SPAC12B10.15c)
no DO ID for congenital_disorder_of_glycosylation_type_iii -> COG5 (SPBC19G7.14c)
no DO ID for corpus_callosum_agenesis_of_with_mental_retardation_ocular_coloboma_and_micrognathia_2 -> IGBP1 (SPCC63.05)
no DO ID for ehlers_danlos_syndrome_spondylodysplastic_type_3 -> SLC39A13 (SPAP8A3.03)
no DO ID for fontaine_progeroid_syndrome -> SLC25A24 (SPBC12D12.05c)
no DO ID for hyperinsulinemic_hypoglycemia_familial_7 -> SLC16A1 (SPAC2G11.13)
no DO ID for immunodeficiency_54 -> MCM4 (SPCC16A11.17)
no DO ID for platelet_activating_factor_acetylhydrolase_deficiency -> PLA2G7 (SPBC106.11c)
no DO ID for pheochromocytoma -> SDHD (SPBP23A10.16)
no DO ID for lujan_fryns_syndrome_2 -> MED12 (SPAC688.08)
no DO ID for myopia_6 -> SCO2 (SPBC119.06)
no DO ID for hyperglycinuria -> SLC36A2 (SPAC3H1.09c)
no DO ID for lynch_syndrome_i -> MSH2 (SPBC19G7.01c)
no DO ID for charcot_marie_tooth_disease_axonal_autosomal_recessive_type_2a2b -> MFN2 (SPBC1706.03)
no DO ID for pigmented_nodular_adrenocortical_disease_primary_4 -> PRKACA (SPBC106.10)
no DO ID for pontocerebellar_hypoplasia_type_2f -> TSEN15 (SPAC959.10)
no DO ID for renal_tubular_acidosis_distal_autosomal_recessive -> ATP6V0A4 (SPAC16E8.07c)
no DO ID for congenital_contractures_of_the_limbs_and_face_hypotonia_and_developmental_delay -> NALCN (SPAC6F6.01)
no DO ID for glaucoma_1_open_angle_g -> WDR36 (SPCC1672.07)
no DO ID for short_stature_microcephaly_and_endocrine_dysfunction -> XRCC4 (SPAC6G9.16c)
no DO ID for aicardi_goutieres_syndrome_4 -> RNASEH2A (SPAC4G9.02)
no DO ID for paragangliomas_1 -> SDHD (SPBP23A10.16)
no DO ID for anemia_sideroblastic_2_pyridoxine_refractory -> SLC25A38 (SPAC823.10c)
no DO ID for diamond_blackfan_anemia_10 -> RPS26 (SPAC1805.11c)
no DO ID for bone_marrow_failure_syndrome_3 -> DNAJC21 (SPAC6B12.08)
no DO ID for mental_retardation_x_linked_12 -> THOC2 (SPAC1D4.14)
no DO ID for meier_gorlin_syndrome_3 -> ORC6 (SPBC2A9.12)
no DO ID for hypophosphatemic_rickets_x_linked_recessive -> CLCN5 (SPBC887.02)
no DO ID for hyperparathyroidism_1 -> CDC73 (SPBC17G9.02c)
no DO ID for antley_bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis -> POR (SPBC29A10.01)
no DO ID for granulomatous_disease_chronic_x_linked -> CYBB (SPBC1683.09c)
no DO ID for disordered_steroidogenesis_due_to_cytochrome_p450_oxidoreductase_deficiency -> POR (SPBC29A10.01)
no DO ID for epileptic_encephalopathy_early_infantile_53 -> SYNJ1 (SPBC2G2.02)
no DO ID for amyotrophic_lateral_sclerosis_15_with_or_without_frontotemporal_dementia_2 -> UBQLN2 (SPAC26A3.16)
no DO ID for pulmonary_fibrosis_and_or_bone_marrow_failure_telomere_related_4 -> PARN (SPBC29A10.09c)
no DO ID for epileptic_encephalopathy_early_infantile_25 -> SLC13A5 (SPBC3B8.04c)
no DO ID for progressive_external_ophthalmoplegia_with_mitochondrial_dna_deletions_autosomal_dominant_1 -> POLG (SPCC24B10.22)
no DO ID for amyotrophic_lateral_sclerosis_22_with_or_without_frontotemporal_dementia -> TUBA4A (SPBC16A3.15c)
no DO ID for cardioencephalomyopathy_fatal_infantile_due_to_cytochrome_c_oxidase_deficiency_4 -> COA6 (SPBC24C6.13)
no DO ID for renal_tubular_acidosis_distal_with_progressive_nerve_deafness -> ATP6V1B1 (SPAC637.05c)
no DO ID for progressive_external_ophthalmoplegia_with_mitochondrial_dna_deletions_autosomal_dominant_2 -> SLC25A4 (SPBC530.10c)
no DO ID for spastic_paraplegia_78_autosomal_recessive -> ATP13A2 (SPCC1672.11c)
no DO ID for epilepsy_early_onset_vitamin_b6_dependent -> PLPBP (SPAC644.09)
no DO ID for cornelia_de_lange_syndrome_4 -> RAD21 (SPCC338.17c)
no DO ID for diamond_blackfan_anemia_1 -> RPS19 (SPBC21C3.13)
no DO ID for encephalopathy_progressive_early_onset_with_brain_edema_and_or_leukoencephalopathy -> NAXE (SPAC15A10.05c)
no DO ID for spondyloepiphyseal_dysplasia_tarda_x_linked -> TRAPPC2 (SPBC11G11.04)
no DO ID for cardioencephalomyopathy_fatal_infantile_due_to_cytochrome_c_oxidase_deficiency_2 -> COX15 (SPAC22E12.10c)
no DO ID for dyschromatosis_universalis_hereditaria_3 -> ABCB6 (SPCC737.09c)
no DO ID for epileptic_encephalopathy_early_infantile_44 -> UBA5 (SPAC1A6.10)
no DO ID for atrioventricular_septal_defect_5 -> GATA6 (SPCC1902.01)
no DO ID for paroxysmal_nocturnal_hemoglobinuria_1 -> PIGA (SPBC3D6.07)
no DO ID for cowden_syndrome_6 -> AKT1 (SPCC24B10.07)
no DO ID for epilepsy_familial_focal_with_variable_foci_2_2 -> NPRL2 (SPAC23H3.03c)
no DO ID for baraitser_winter_syndrome_2 -> ACTG1 (SPBC32H8.12c)
no DO ID for basal_ganglia_calcification_idiopathic_6 -> XPR1 (SPAC227.01c)
no DO ID for hypotonia_infantile_with_psychomotor_retardation_and_characteristic_facies_1 -> NALCN (SPAC6F6.01)
no DO ID for coenzyme_q10_deficiency_primary_1 -> COQ2 (SPAC56F8.04c)
no DO ID for alacrima_achalasia_and_mental_retardation_syndrome -> GMPPA (SPBC13G1.02)
no DO ID for peroxisome_biogenesis_disorder_6b -> PEX10 (SPBC17A3.10)
no DO ID for hyperphosphatasia_with_mental_retardation_syndrome_4 -> PGAP3 (SPAC823.07)
no DO ID for optic_atrophy_10_with_or_without_ataxia_mental_retardation_and_seizures -> RTN4IP1 (SPBC16A3.02c)
no DO ID for periventricular_nodular_heterotopia_7 -> NEDD4L (SPAC11G7.02)
no DO ID for advanced_sleep_phase_syndrome_familial_2_2 -> CSNK1D (SPAC23C4.12)
no DO ID for microcephaly_short_stature_and_impaired_glucose_metabolism_1 -> TRMT10A (SPAC6B12.09)
no DO ID for d_2_hydroxyglutaric_aciduria_2 -> IDH2 (SPAC6G10.08)
no DO ID for epileptic_encephalopathy_early_infantile_51 -> MDH2 (SPCC306.08c)
no DO ID for peroxisome_biogenesis_disorder_4a -> PEX6 (SPAC17A5.01)
no DO ID for peroxisome_biogenesis_disorder_3a -> PEX12 (SPAPB17E12.03)
no DO ID for polymicrogyria_perisylvian_with_cerebellar_hypoplasia_and_arthrogryposis -> PI4KA (SPBC577.06c)
no DO ID for meier_gorlin_syndrome_4 -> CDT1 (SPBC428.18)
no DO ID for mental_retardation_x_linked_49_2 -> CLCN4 (SPBC887.02)
no DO ID for treacher_collins_syndrome_2 -> POLR1D (SPAC1687.01)
no DO ID for peroxisome_biogenesis_disorder_8b -> PEX16 (SPBC646.15c)
no DO ID for muscular_dystrophy_congenital_davignon_chauveau_type -> TRIP4 (SPAC1A6.01c)
no DO ID for deafness_x_linked_1 -> PRPS1 (SPCC1620.06c)
no DO ID for cole_carpenter_syndrome_2 -> SEC24D (SPBC4.03c)
no DO ID for heimler_syndrome_2 -> PEX6 (SPAC17A5.01)
no DO ID for leukoencephalopathy_progressive_with_ovarian_failure -> AARS2 (SPAC23C11.09)
no DO ID for diamond_blackfan_anemia_13 -> RPS29 (SPBC1685.09)
no DO ID for microphthalmia_isolated_with_coloboma_7_2 -> ABCB6 (SPCC737.09c)
no DO ID for diamond_blackfan_anemia_7 -> RPL11 (SPBC17G9.10)
no DO ID for peroxisome_biogenesis_disorder_11b -> PEX13 (SPAC3C7.10)
no DO ID for diamond_blackfan_anemia_5 -> RPL35A (SPCP31B10.08c)
no DO ID for adams_oliver_syndrome_3 -> RBPJ (SPCC1223.13)
no DO ID for hyperphosphatasia_with_mental_retardation_syndrome_6 -> PIGY (SPAC227.19c)
no DO ID for combined_oxidative_phosphorylation_deficiency_29 -> TXN2 (SPAC7D4.07c)
no DO ID for zimmermann_laband_syndrome_2 -> ATP6V1B2 (SPAC637.05c)
no DO ID for al_raqad_syndrome -> DCPS (SPBP4H10.20)
no DO ID for cardiofaciocutaneous_syndrome_4 -> MAP2K2 (SPAC1D4.13)
no DO ID for cole_carpenter_syndrome_1 -> P4HB (SPAC1F5.02)
no DO ID for mental_retardation_autosomal_recessive_5_2 -> NSUN2 (SPAC23C4.17)
no DO ID for cardiofaciocutaneous_syndrome_3 -> MAP2K1 (SPAC1D4.13)
no DO ID for peroxisome_biogenesis_disorder_10a -> PEX3 (SPAC29A4.14c)
no DO ID for uv_sensitive_syndrome_2_2 -> ERCC8 (SPBC577.09)
no DO ID for spermatogenic_failure_3 -> SLC26A8 (SPBC3H7.02)
no DO ID for mental_retardation_autosomal_recessive_14 -> TECR (SPBC646.07c)
no DO ID for trichothiodystrophy_3_photosensitive -> GTF2H5 (SPBC32F12.15)
no DO ID for cowden_syndrome_7 -> SEC23B (SPBC776.04)
no DO ID for trichothiodystrophy_2_photosensitive -> ERCC3 (SPAC17A5.06)
no DO ID for mental_retardation_autosomal_recessive_55 -> PUS3 (SPAC25B8.05)
no DO ID for microcephaly_4_primary_autosomal_recessive -> KNL1 (SPCC1020.02)
no DO ID for conotruncal_heart_malformations -> GATA6 (SPCC1902.01)
no DO ID for trichohepatoenteric_syndrome_2 -> SKIV2L (SPCC550.03c)
no DO ID for thrombocytopenia_4 -> CYCS (SPCC191.07)
no DO ID for paragangliomas_2 -> SDHAF2 (SPAC12B10.06c)
no DO ID for colorectal_cancer_hereditary_nonpolyposis_type_4 -> PMS2 (SPAC19G12.02c)
no DO ID for colorectal_cancer_hereditary_nonpolyposis_type_5 -> MSH6 (SPCC285.16c)
no DO ID for muscular_dystrophy_dystroglycanopathy_congenital_with_brain_and_eye_anomalies_type_a_1 -> POMT1 (SPBC16C6.09)
no DO ID for muscular_dystrophy_dystroglycanopathy_type_a_11 -> B3GALNT2 (SPBC1921.06c)
no DO ID for muscular_dystrophy_dystroglycanopathy_type_a_14 -> GMPPB (SPCC1906.01)
no DO ID for muscular_dystrophy_dystroglycanopathy_congenital_with_brain_and_eye_anomalies_type_a_2 -> POMT2 (SPAC22A12.07c)
no DO ID for muscular_dystrophy_dystroglycanopathy_congenital_with_mental_retardation_type_b_1 -> POMT1 (SPBC16C6.09)
no DO ID for muscular_dystrophy_dystroglycanopathy_type_b_14 -> GMPPB (SPCC1906.01)
no DO ID for muscular_dystrophy_dystroglycanopathy_congenital_with_mental_retardation_type_b_2 -> POMT2 (SPAC22A12.07c)
no DO ID for neuronopathy_distal_hereditary_motor_type_viib -> DCTN1 (SPAC27D7.13c)
no DO ID for fibrosis_of_extraocular_muscles_congenital_3a_with_or_without_extraocular_involvement -> TUBB3 (SPBC26H8.07c)
no DO ID for generalized_epilepsy_with_febrile_seizures_plus_type_9 -> STX1B (SPCC825.03c)
no DO ID for myopathy_lactic_acidosis_and_sideroblastic_anemia_2 -> YARS2 (SPCC576.06c)
no DO ID for proteinuria_low_molecular_weight_with_hypercalciuria_and_nephrocalcinosis -> CLCN5 (SPBC887.02)
no DO ID for cholestasis_intrahepatic_of_pregnancy_3_2 -> ABCB4 (SPCC663.03)
no DO ID for nephrotic_syndrome_type_9 -> COQ8B (SPBC2D10.18)
no DO ID for premature_ovarian_failure_11 -> ERCC6 (SPCP25A2.02c)
no DO ID for hyperuricemic_nephropathy_familial_juvenile_4 -> SEC61A1 (SPBC19G7.17)
no DO ID for nephrotic_syndrome_type_12_2 -> NUP93 (SPCC1620.11)
no DO ID for adenosine_triphosphate_elevated_of_erythrocytes -> PKLR (SPAC4H3.10c)
no DO ID for nephrotic_syndrome_type_11_2 -> NUP107 (SPBC428.01c)
no DO ID for pontocerebellar_hypoplasia_type_1c -> EXOSC8 (SPBC17D1.03c)
no DO ID for trichothiodystrophy_6_nonphotosensitive -> GTF2E2 (SPCC1672.08c)
no DO ID for cerebrooculofacioskeletal_syndrome_4 -> ERCC1 (SPBC4F6.15c)
no DO ID for focal_cortical_dysplasia_type_ii -> TSC2 (SPAC18B11.11)
no DO ID for striatonigral_degeneration_infantile_2 -> NUP62 (SPAC26A3.15c)
no DO ID for developmental_delay_with_short_stature_dysmorphic_features_and_sparse_hair -> DPH1 (SPBC3B8.05)
no DO ID for au_kline_syndrome -> HNRNPK (SPCC757.09c)
no DO ID for arterial_calcification_generalized_of_infancy_2 -> ABCC6 (SPAC30.04c)
no DO ID for congenital_disorder_of_glycosylation_type_it -> PGM1 (SPBC32F12.10)
no DO ID for factor_v_and_factor_viii_combined_deficiency_of_1 -> LMAN1 (SPBC4F6.05c)
no DO ID for mental_retardation_x_linked_syndromic_cabezas_type -> CUL4B (SPAC3A11.08)
no DO ID for methemoglobinemia_due_to_deficiency_of_methemoglobin_reductase -> CYB5R3 (SPCC970.03)
no DO ID for mitochondrial_dna_depletion_syndrome_12a_autosomal_dominant -> SLC25A4 (SPBC530.10c)
no DO ID for mitochondrial_dna_depletion_syndrome_12b_autosomal_recessive -> SLC25A4 (SPBC530.10c)
no DO ID for neuronopathy_distal_hereditary_motor_type_iia -> HSPB8 (SPCC338.06c)
no DO ID for neuronopathy_distal_hereditary_motor_type_iib -> HSPB1 (SPCC338.06c)
no DO ID for deafness_dystonia_and_cerebral_hypomyelination -> BCAP31 (SPAC9E9.04)
no DO ID for monocarboxylate_transporter_1_deficiency -> SLC16A1 (SPAC2G11.13)
no DO ID for exocrine_pancreatic_insufficiency_dyserythropoietic_anemia_and_calvarial_hyperostosis -> COX4I2 (SPCC338.10c)
no DO ID for intellectual_developmental_disorder_with_dysmorphic_facies_seizures_and_distal_limb_anomalies -> OTUD6B (SPAC1952.03)
no DO ID for neuropathy_hereditary_sensory_with_spastic_paraplegia_autosomal_recessive -> CCT5 (SPAC1420.02c)
no DO ID for cerebellar_atrophy_visual_impairment_and_psychomotor_retardation -> EMC1 (SPAC25H1.07)
no DO ID for pituitary_adenoma_4_acth_secreting -> USP8 (SPBC18H10.08c)
no DO ID for sudden_cardiac_failure_alcohol_induced -> PPA2 (SPAC3A12.02)
no DO ID for facial_palsy_congenital_with_ptosis_and_velopharyngeal_dysfunction -> TUBB6 (SPBC26H8.07c)
no DO ID for exercise_intolerance_riboflavin_responsive -> SLC25A32 (SPBC27B12.09c)
no DO ID for retinitis_pigmentosa_with_or_without_skeletal_anomalies -> CWC27 (SPBC16H5.05c)
no DO ID for coenzyme_q10_deficiency_primary_8 -> COQ7 (SPBC337.15c)
no DO ID for mental_retardation_autosomal_recessive_52 -> LMAN2L (SPCC126.08c)
no DO ID for deafness_autosomal_dominant_71 -> DMXL2 (SPBC1105.10)
no DO ID for neurodevelopmental_disorder_with_microcephaly_ataxia_and_seizures -> SARS (SPAC29A4.15)
no DO ID for mental_retardation_autosomal_recessive_50 -> EDC3 (SPBC18E5.11c)
no DO ID for hypotonia_infantile_with_psychomotor_retardation -> CCDC174 (SPAC140.04)
no DO ID for ck_syndrome -> NSDHL (SPBC3F6.02c)
no DO ID for trehalase_deficiency -> TREH (SPBC660.07)
no DO ID for short_stature_hearing_loss_retinitis_pigmentosa_and_distinctive_facies -> EXOSC2 (SPAC2F7.14c)
no DO ID for mental_retardation_x_linked_syndromic_christianson_type_2 -> SLC9A6 (SPAC15A10.06)
no DO ID for focal_facial_dermal_dysplasia_4 -> CYP26C1 (SPAC19A8.04)
no DO ID for spermatogenic_failure_5 -> AURKC (SPCC320.13c)
no DO ID for immunodeficiency_55 -> GINS1 (SPBP23A10.09)
no DO ID for cockayne_syndrome_a -> ERCC8 (SPBC577.09)
no DO ID for inclusion_body_myopathy_with_early_onset_paget_disease_with_or_without_frontotemporal_dementia_1 -> VCP (SPAC1565.08)
no DO ID for cornelia_de_lange_syndrome_2 -> SMC1A (SPBC29A10.04)
no DO ID for neurodevelopmental_disorder_with_microcephaly_hypotonia_and_variable_brain_anomalies -> PRUNE1 (SPAC2F3.11)
no DO ID for galactose_epimerase_deficiency -> GALE (SPBPB2B2.12c)
no DO ID for epileptic_encephalopathy_early_infantile_4 -> STXBP1 (SPCC584.05)
no DO ID for encephalopathy_neonatal_severe_with_lactic_acidosis_and_brain_abnormalities -> LIPT2 (SPAC4F10.05c)
no DO ID for myopathy_congenital_with_fiber_type_disproportion -> TPM3 (SPAC27F1.02c)
no DO ID for epileptic_encephalopathy_early_infantile_17 -> GNAO1 (SPBC24C6.06)
no DO ID for epileptic_encephalopathy_early_infantile_38 -> ARV1 (SPAPB1A10.15)
no DO ID for myopathy_myosin_storage_autosomal_dominant -> MYH7 (SPCC645.05c)
no DO ID for peroxisome_biogenesis_disorder_1a -> PEX1 (SPCC553.03)
no DO ID for epileptic_encephalopathy_early_infantile_3 -> SLC25A22 (SPCC1682.09c)
no DO ID for 3_methylglutaconic_aciduria_type_ix -> TIMM50 (SPBC17A3.01c)
no DO ID for congenital_disorder_of_glycosylation_type_iig -> COG1 (SPAC144.15c)
no DO ID for schimmelpenning_feuerstein_mims_syndrome -> KRAS (SPAC17H9.09c)
no DO ID for duane_retraction_syndrome_2 -> CHN1 (SPBC23G7.08c)
no DO ID for oocyte_maturation_defect_2 -> TUBB8 (SPBC26H8.07c)
no DO ID for retinitis_pigmentosa_77 -> REEP6 (SPCC830.08c)
no DO ID for neurodevelopmental_disorder_mitochondrial_with_abnormal_movements_and_lactic_acidosis_with_or_without_seizures -> WARS2 (SPAC3G9.13c)
no DO ID for congenital_heart_defects_dysmorphic_facial_features_and_intellectual_developmental_disorder -> CDK13 (SPAC2F3.15)
no DO ID for cardioencephalomyopathy_fatal_infantile_due_to_cytochrome_c_oxidase_deficiency_1 -> SCO2 (SPBC119.06)
no DO ID for noonan_syndrome_like_disorder_with_loose_anagen_hair_2 -> PPP1CB (SPBC776.02c)
no DO ID for language_delay_and_attention_deficit_hyperactivity_disorder_cognitive_impairment_with_or_without_cardiac_arrhythmia -> GNB5 (SPBC32H8.07)
no DO ID for growth_retardation_intellectual_developmental_disorder_hypotonia_and_hepatopathy -> IARS (SPBC8D2.06)
no DO ID for skin_creases_congenital_symmetric_circumferential_2 -> MAPRE2 (SPAC18G6.15)
no DO ID for intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis -> BRPF1 (SPBC17D11.04c)
no DO ID for midface_hypoplasia_hearing_impairment_elliptocytosis_and_nephrocalcinosis -> AMMECR1 (SPAC688.03c)
no DO ID for combined_oxidative_phosphorylation_deficiency_33 -> C1QBP (SPBC776.07)
no DO ID for okur_chung_neurodevelopmental_syndrome -> CSNK2A1 (SPAC23C11.11)
no DO ID for cerebroretinal_microangiopathy_with_calcifications_and_cysts_2 -> STN1 (SPBC409.12c)
no DO ID for skin_creases_congenital_symmetric_circumferential_1 -> TUBB (SPBC26H8.07c)
no DO ID for porokeratosis_7_multiple_types -> MVD (SPAC24C9.03)
no DO ID for neurodevelopmental_disorder_with_progressive_microcephaly_spasticity_and_brain_anomalies -> PLAA (SPBC887.04c)
no DO ID for lung_disease_immunodeficiency_and_chromosome_breakage_syndrome -> NSMCE3 (SPCC645.04)
no DO ID for sudden_cardiac_failure_infantile -> PPA2 (SPAC3A12.02)
no DO ID for galloway_mowat_syndrome_2_x_linked -> LAGE3 (SPAC4H3.13)
no DO ID for peroxisome_biogenesis_disorder_3b -> PEX12 (SPAPB17E12.03)
no DO ID for myopathy_due_to_myoadenylate_deaminase_deficiency -> AMPD1 (SPBC106.04)
no DO ID for cerebral_palsy_spastic_quadriplegic_3 -> ADD3 (SPBC359.06)
no DO ID for auditory_neuropathy_and_optic_atrophy -> FDXR (SPBC3B8.01c)
no DO ID for epileptic_encephalopathy_early_infantile_56 -> YWHAG (SPAC17A2.13c)
no DO ID for spermatogenic_failure_16 -> SUN5 (SPBC12D12.01)
no DO ID for myopathy_congenital_with_fiber_type_disproportion -> ACTA1 (SPBC32H8.12c)
no DO ID for pilarowski_bjornsson_syndrome -> CHD1 (SPAC3G6.01)
no DO ID for mental_retardation_autosomal_recessive_60 -> TAF13 (SPCC1494.02c)
no DO ID for cardiac_valvular_defect_developmental -> PLD1 (SPAC2F7.16c)
no DO ID for anauxetic_dysplasia_2 -> POP1 (SPAC25B8.16)
no DO ID for brachycephaly_trichomegaly_and_developmental_delay -> RPS23 (SPBP4H10.13)
no DO ID for porokeratosis_9_multiple_types -> FDPS (SPBC36.06c)
no DO ID for diamond_blackfan_anemia_6 -> RPL5 (SPBC11C11.09c)
no DO ID for deafness_autosomal_recessive_107 -> WBP2 (SPAC29B12.11c)
no DO ID for peroxisome_biogenesis_disorder_2b -> PEX5 (SPBC725.07)
no DO ID for congenital_disorder_of_glycosylation_type_il -> ALG9 (SPAC1834.05)
no DO ID for heimler_syndrome_1 -> PEX1 (SPCC553.03)
no DO ID for colorectal_cancer_hereditary_nonpolyposis_type_2 -> MLH1 (SPBC1703.04)
no DO ID for parkinson_disease_22_autosomal_dominant -> CHCHD2 (SPAC6C3.02c)
no DO ID for neuronopathy_distal_hereditary_motor_type_ix -> WARS (SPAC2F7.13c)
no DO ID for cerebrooculofacioskeletal_syndrome_1 -> ERCC6 (SPCP25A2.02c)
no DO ID for neurodegeneration_childhood_onset_with_brain_atrophy -> UBTF (SPBC28F2.11)
no DO ID for schimmelpenning_feuerstein_mims_syndrome -> HRAS (SPAC17H9.09c)
no DO ID for glycosylphosphatidylinositol_biosynthesis_defect_11 -> PIGW (SPAC144.10c)
no DO ID for neuronopathy_distal_hereditary_motor_type_va -> GARS (SPAC3F10.03)
no DO ID for neuronopathy_distal_hereditary_motor_type_va -> BSCL2 (SPAC3A11.04)
no DO ID for pseudohyperkalemia_familial_2_due_to_red_cell_leak -> ABCB6 (SPCC737.09c)
no DO ID for neuropathy_ataxia_and_retinitis_pigmentosa -> MT-ATP6 (SPMIT.07)
no DO ID for breast_ovarian_cancer_familial_4 -> RAD51D (SPAC3C7.03c)
no DO ID for colchicine_resistance -> ABCB1 (SPCC663.03)
no DO ID for peroxisome_biogenesis_disorder_14b -> PEX11B (SPBC582.09)
no DO ID for microphthalmia_syndromic_13 -> HMGB3 (SPAC4G9.11c)
no DO ID for rhabdoid_tumor_predisposition_syndrome_2 -> SMARCA4 (SPCC1620.14c)
no DO ID for wiskott_aldrich_syndrome_2 -> WIPF1 (SPBC13E7.09)
no DO ID for diamond_blackfan_anemia_17 -> RPS27 (SPBC1685.10)
no DO ID for diamond_blackfan_anemia_16 -> RPL27 (SPCC74.05)
no DO ID for diamond_blackfan_anemia_11 -> RPL26 (SPBC29B5.03c)
no DO ID for hermansky_pudlak_syndrome_10 -> AP3D1 (SPAC144.06)
no DO ID for lissencephaly_7_with_cerebellar_hypoplasia -> CDK5 (SPCC16C4.11)
no DO ID for schwannomatosis_1_2 -> SMARCB1 (SPCC16A11.14)
no DO ID for diamond_blackfan_anemia_12 -> RPL15 (SPCC576.11)
no DO ID for coronary_artery_disease_autosomal_dominant_1 -> MEF2A (SPBC19G7.06)
no DO ID for premature_ovarian_failure_2a -> DIAPH2 (SPCC895.05)
no DO ID for diabetes_mellitus_noninsulin_dependent_5 -> TBC1D4 (SPCC1620.12c)
no DO ID for orofacial_cleft_10 -> SUMO1 (SPBC365.06)
no DO ID for ventricular_fibrillation_paroxysmal_familial_2 -> DPP6 (SPACUNK4.08)
no DO ID for trichothiodystrophy_5_nonphotosensitive -> RNF113A (SPBC13E7.02)
no DO ID for paragangliomas_3 -> SDHC (SPCC330.12c)
no DO ID for mental_retardation_autosomal_recessive_58 -> ELP2 (SPCC895.06)
no DO ID for neuronopathy_distal_hereditary_motor_type_vb -> REEP1 (SPBC30D10.09c)
no DO ID for burn_mckeown_syndrome -> TXNL4A (SPCC16A11.05c)
no DO ID for stargardt_disease_3 -> ELOVL4 (SPAC1639.01c)
no DO ID for microcephaly_3_primary_autosomal_recessive -> CDK5RAP2 (SPCC417.07c)
no DO ID for short_rib_thoracic_dysplasia_17_with_or_without_polydactyly -> TCTEX1D2 (SPAC1805.08)
no DO ID for greenberg_dysplasia -> LBR (SPBC16G5.18)
no DO ID for diamond_blackfan_anemia_4 -> RPS17 (SPBC839.05c)
no DO ID for epilepsy_familial_focal_with_variable_foci_3 -> NPRL3 (SPBC543.04)
no DO ID for cornelia_de_lange_syndrome_3 -> SMC3 (SPAC10F6.09c)
no DO ID for luscan_lumish_syndrome -> SETD2 (SPAC29B12.02c)
no DO ID for cowden_syndrome_3 -> SDHD (SPBP23A10.16)
no DO ID for mental_retardation_autosomal_recessive_42 -> PGAP1 (SPAC824.02)
no DO ID for peroxisome_biogenesis_disorder_6a -> PEX10 (SPBC17A3.10)
no DO ID for diamond_blackfan_anemia_15_with_mandibulofacial_dysostosis_2 -> RPS28 (SPCC285.15c)
no DO ID for de_sanctis_cacchione_syndrome -> ERCC6 (SPCP25A2.02c)
no DO ID for epileptic_encephalopathy_early_infantile_48 -> AP3B2 (SPAC23H3.06)
no DO ID for retinitis_pigmentosa_and_erythrocytic_microcytosis -> TRNT1 (SPCC645.10)
no DO ID for myoglobinuria_acute_recurrent_autosomal_recessive -> LPIN1 (SPAC1952.13)
no DO ID for gillessen_kaesbach_nishimura_syndrome -> ALG9 (SPAC1834.05)
no DO ID for peroxisome_biogenesis_disorder_4b -> PEX6 (SPAC17A5.01)
no DO ID for diamond_blackfan_anemia_8 -> RPS7 (SPAC18G6.14c)
no DO ID for kabuki_syndrome_2 -> KDM6A (SPBC23E6.09)
no DO ID for peroxisome_biogenesis_disorder_11a -> PEX13 (SPAC3C7.10)
no DO ID for microcephaly_and_chorioretinopathy_autosomal_recessive_3 -> TUBGCP4 (SPBC211.06)
no DO ID for diamond_blackfan_anemia_3 -> RPS24 (SPBC17G9.07)
no DO ID for diamond_blackfan_anemia_9 -> RPS10 (SPBP22H7.08)
no DO ID for mental_retardation_autosomal_recessive_44 -> METTL23 (SPAC3A11.03)
no DO ID for premature_ovarian_failure_8 -> STAG3 (SPAC17H9.20)
no DO ID for peroxisome_biogenesis_disorder_13a -> PEX14 (SPBC13G1.03c)
no DO ID for peroxisome_biogenesis_disorder_8a_2 -> PEX16 (SPBC646.15c)
no DO ID for mirror_movements_2 -> RAD51 (SPAC644.14c)
no DO ID for specific_granule_deficiency_2 -> SMARCD2 (SPAC23G3.10c)
no DO ID for mental_retardation_autosomal_recessive_56 -> ZC3H14 (SPAC14C4.06c)
no DO ID for nephrotic_syndrome_type_8 -> ARHGDIA (SPAC6F12.06)
no DO ID for anemia_sideroblastic_4 -> HSPA9 (SPAC664.11)
no DO ID for peroxisome_biogenesis_disorder_2a -> PEX5 (SPBC725.07)
no DO ID for rhabdomyosarcoma_embryonal_2 -> DICER1 (SPCC188.13c)
no DO ID for retinitis_pigmentosa_79 -> HK1 (SPAC4F8.07c)
no DO ID for progressive_external_ophthalmoplegia_with_mitochondrial_dna_deletions_autosomal_dominant_5 -> RRM2B (SPBC25D12.04)
no DO ID for meier_gorlin_syndrome_7 -> CDC45 (SPAC17D4.02)
no DO ID for polycystic_liver_disease_1_with_or_without_kidney_cysts -> PRKCSH (SPCC825.02)
no DO ID for cone_rod_dystrophy_21 -> DRAM2 (SPCC16A11.01)
no DO ID for pseudoxanthoma_elasticum_forme_fruste -> ABCC6 (SPAC30.04c)
no DO ID for congenital_disorder_of_glycosylation_type_iq -> SRD5A3 (SPAC7D4.09c)
no DO ID for peroxisome_biogenesis_disorder_12a -> PEX19 (SPAC17C9.14)
no DO ID for epileptic_encephalopathy_early_infantile_12 -> PLCB1 (SPAC22F8.11)
no DO ID for jawad_syndrome -> RBBP8 (SPCC338.08)
no DO ID for neurodevelopmental_disorder_with_microcephaly_epilepsy_and_brain_atrophy -> TRAPPC6B (SPAC13G6.05c)
no DO ID for ovarian_dysgenesis_3 -> PSMC3IP (SPAC222.15)
no DO ID for cerebrooculofacioskeletal_syndrome_3 -> ERCC5 (SPBC3E7.08c)
no DO ID for colorectal_cancer_10 -> POLD1 (SPBC336.04)
no DO ID for melanoma_cutaneous_malignant_10 -> POT1 (SPAC26H5.06)
no DO ID for paraganglioma_and_gastric_stromal_sarcoma -> SDHC (SPCC330.12c)
no DO ID for sick_sinus_syndrome_3 -> MYH6 (SPCC645.05c)
no DO ID for psoriasis_15_pustular -> AP1S3 (SPAP27G11.06c)
no DO ID for autism_x_linked_5_2 -> RPL10 (SPBC18E5.04)
no DO ID for ovalocytosis_southeast_asian -> SLC4A1 (SPBC543.05c)
no DO ID for melanoma_cutaneous_malignant_6 -> XRCC3 (SPAC20H4.07)
no DO ID for aspartate_aminotransferase_serum_level_of_quantitative_trait_locus_1 -> GOT1 (SPAC10F6.13c)
no DO ID for mental_retardation_fra12a_type -> DIP2B (SPAC56F8.02)
no DO ID for methemoglobinemia_and_ambiguous_genitalia -> CYB5A (SPCC16A11.10c)
no DO ID for periventricular_heterotopia_with_microcephaly_autosomal_recessive -> ARFGEF2 (SPAC4D7.01c)
no DO ID for polycystic_liver_disease_2_with_or_without_kidney_cysts -> SEC63 (SPBC36B7.03)
no DO ID for glioma_susceptibility_9 -> POT1 (SPAC26H5.06)
no DO ID for erythrocyte_amp_deaminase_deficiency -> AMPD3 (SPBC106.04)
no DO ID for spinocerebellar_ataxia_x_linked_1 -> ATP2B3 (SPAPB2B4.04c)
no DO ID for neural_tube_defects_folate_sensitive -> MTHFD1 (SPBC2G2.08)
no DO ID for spinal_muscular_atrophy_with_congenital_bone_fractures_2 -> ASCC1 (SPBC15D4.13c)
no DO ID for spermatogenic_failure_21 -> BRDT (SPCC1450.02)
no DO ID for shaheen_syndrome -> COG6 (SPBC776.10c)
no DO ID for parkinson_disease_11_autosomal_dominant -> GIGYF2 (SPAC4F10.13c)
no DO ID for parkinson_disease_13_autosomal_dominant -> HTRA2 (SPAC23G3.12c)
no DO ID for myopathy_myofibrillar_fatal_infantile_hypertonic_alpha_b_crystallin_related -> CRYAB (SPCC338.06c)
no DO ID for fanconi_anemia_complementation_group_w -> RFWD3 (SPAC343.18)
no DO ID for glioma_susceptibility_2 -> PTEN (SPBC609.02)
no DO ID for mental_retardation_x_linked_107 -> CXorf56 (SPBC839.19)
no DO ID for microcephaly_19_primary_autosomal_recessive -> COPB2 (SPBC16C6.13c)
no DO ID for microcephaly_21_primary_autosomal_recessive -> NCAPD2 (SPBC776.13)
no DO ID for microcephaly_23_primary_autosomal_recessive -> NCAPH (SPCC306.03c)
no DO ID for neurodevelopmental_disorder_with_brain_liver_and_lung_abnormalities -> FARSB (SPAC23A1.12c)
no DO ID for neuronopathy_distal_hereditary_motor_type_iic -> HSPB3 (SPCC338.06c)
no DO ID for pentosuria -> DCXR (SPAC4H3.08)
no DO ID for basan_syndrome -> SMARCAD1 (SPAC25A8.01c)
no DO ID for short_stature_rhizomelic_with_microcephaly_micrognathia_and_developmental_delay -> ARCN1 (SPCC285.08)
no DO ID for platelet_abnormalities_with_eosinophilia_and_immune_mediated_inflammatory_disease -> ARPC1B (SPBC14C8.06)
no DO ID for epileptic_encephalopathy_infantile_or_early_childhood_1 -> PPP3CA (SPBP4H10.04)
no DO ID for epileptic_encephalopathy_early_infantile_29 -> AARS (SPAC23C11.09)
no DO ID for intellectual_developmental_disorder_with_cardiac_arrhythmia -> GNB5 (SPBC32H8.07)
no DO ID for skraban_deardorff_syndrome -> WDR26 (SPAC343.04c)
no DO ID for mental_retardation_autosomal_recessive_59 -> IMPA1 (SPCC1753.04)
no DO ID for stankiewicz_isidor_syndrome -> PSMD12 (SPAC1420.03)
no DO ID for myosin_storage_myopathy -> MYH7 (SPCC645.05c)
no DO ID for neurodevelopmental_disorder_with_spastic_quadriplegia_and_brain_abnormalities_with_or_without_seizures -> WDR45B (SPAC458.06)
no DO ID for schimmelpenning_feuerstein_mims_syndrome -> NRAS (SPAC17H9.09c)
no DO ID for polycystic_liver_disease_3_with_or_without_kidney_cysts -> ALG8 (SPAC17C9.07)
no DO ID for combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia -> MTHFD1 (SPBC2G2.08)
no DO ID for glycosylphosphatidylinositol_biosynthesis_defect_15 -> GPAA1 (SPAC1002.11)
no DO ID for mental_retardation_x_linked_syndromic_houge_type -> CNKSR2 (SPBC1289.04c)
no DO ID for microcephaly_and_chorioretinopathy_autosomal_recessive_1 -> TUBGCP6 (SPCC4G3.19)
no DO ID for uv_sensitive_syndrome_1 -> ERCC6 (SPCP25A2.02c)
no DO ID for glycosylphosphatidylinositol_biosynthesis_defect_16 -> PIGC (SPCC550.04c)
no DO ID for combined_oxidative_phosphorylation_deficiency_36 -> MRPS2 (SPAC24C9.10c)
no DO ID for developmental_delay_and_seizures_with_or_without_movement_abnormalities -> DHDDS (SPAC4D7.04c)
no DO ID for hyperekplexia_4 -> ATAD1 (SPCC24B10.10c)
no DO ID for keratoconus_9 -> TUBA3D (SPBC16A3.15c)
no DO ID for leber_congenital_amaurosis_with_early_onset_deafness -> TUBB4B (SPBC26H8.07c)
no DO ID for leukodystrophy_hypomyelinating_15 -> EPRS (SPAC17A5.15c)
no DO ID for mental_retardation_autosomal_dominant_55_with_seizures -> NUS1 (SPBC2A9.06c)
no DO ID for microcephaly_20_primary_autosomal_recessive -> KIF14 (SPAC144.14)
no DO ID for multiple_mitochondrial_dysfunctions_syndrome_6 -> PMPCB (SPBP23A10.15c)
no DO ID for nephrolithiasis_x_linked_recessive_with_renal_failure -> CLCN5 (SPBC887.02)
no DO ID for neurodevelopmental_disorder_with_ataxic_gait_absent_speech_and_decreased_cortical_white_matter -> RAB11B (SPAC18G6.03)
no DO ID for optic_atrophy_5 -> DNM1L (SPAC767.01c)
no DO ID for rh_null_amorph_type -> RHCE (SPAC2E1P3.02c)
no DO ID for shwachman_diamond_syndrome_2 -> EFL1 (SPCC553.08c)
no DO ID for spinal_muscular_atrophy_type_i_with_congenital_bone_fractures -> TRIP4 (SPAC1A6.01c)
no DO ID for spinocerebellar_ataxia_47 -> PUM1 (SPAC1687.22c)
no DO ID for distal_hereditary_motor_neuropathy_type_v_2 -> GARS (SPAC3F10.03)
no DO ID for epileptic_encephalopathy_early_infantile_55 -> PIGP (SPAC22A12.13)
no DO ID for cockayne_syndrome_type_i -> ERCC8 (SPBC577.09)
no DO ID for deafness_enamel_hypoplasia_nail_defects -> PEX1 (SPCC553.03)
no DO ID for toe_syndactyly_telecanthus_and_anogenital_and_renal_malformations -> CCNQ (SPBC32F12.06)
no DO ID for distal_hereditary_motor_neuropathy_type_v_2 -> BSCL2 (SPAC3A11.04)
no DO ID for carcinoid_tumors_intestinal -> SDHD (SPBP23A10.16)
no DO ID for adenosine_monophosphate_deaminase_1_deficiency -> AMPD1 (SPBC106.04)
no DO ID for autosomal_recessive_chorioretinopathy_microcephaly_syndrome -> TUBGCP6 (SPCC4G3.19)
no DO ID for mosaic_variegated_aneuploidy_syndrome -> CEP57 (SPAC4H3.11c)
no DO ID for hereditary_paraganglioma_pheochromocytoma_syndromes -> SDHB (SPAC140.01)
no DO ID for hereditary_paraganglioma_pheochromocytoma_syndromes -> SDHC (SPCC330.12c)
no DO ID for tuberous_sclerosis_1_2 -> TSC2 (SPAC18B11.11)
no DO ID for cockayne_syndrome_type_ii -> ERCC6 (SPCP25A2.02c)
no DO ID for neonatal_adrenoleukodystrophy -> PEX5 (SPBC725.07)
no DO ID for mosaic_variegated_aneuploidy_syndrome -> BUB1B (SPCC1322.12c)
no DO ID for hereditary_methemoglobinemia -> CYB5R3 (SPCC970.03)
no DO ID for hereditary_paraganglioma_pheochromocytoma_syndromes -> SDHD (SPBP23A10.16)
no DO ID for cerebellar_hypoplasia_with_endosteal_sclerosis -> POLR3B (SPAC4G9.08c)
no DO ID for peho_syndrome -> KIF1A (SPAC144.14)
no DO ID for factor_v_and_factor_viii_combined_deficiency_of_2 -> LMAN1 (SPBC4F6.05c)
no DO ID for hereditary_paraganglioma_pheochromocytoma_syndromes -> SDHAF2 (SPAC12B10.06c)
no DO ID for familial_paroxysmal_nonkinesigenic_dyskinesia -> PNKD (SPAC824.07)
no DO ID for wiedemann_steiner_syndrome -> SMC1A (SPBC29A10.04)
no DO ID for severe_congenital_neutropenia_autosomal_dominant -> TCIRG1 (SPAC16E8.07c)
no DO ID for mitochondrial_neurogastrointestinal_encephalomyopathy -> POLG (SPCC24B10.22)
no DO ID for autosomal_recessive_non_syndromic_sensorineural_deafness_type_dfnb -> SLC26A4 (SPBC3H7.02)
no DO ID for fatal_infantile_cytochrome_c_oxidase_deficiency -> SCO2 (SPBC119.06)
no DO ID for melorheostosis_with_osteopoikilosis -> LEMD3 (SPAC14C4.05c)
no DO ID for multiple_benign_circumferential_skin_creases_on_limbs -> TUBB (SPBC26H8.07c)
no DO ID for x_linked_intellectual_disability_siderius_type -> PHF8 (SPCC622.16c)
no DO ID for myopathy_lactic_acidosis_and_sideroblastic_anemia_3 -> MT-ATP6 (SPMIT.07)
no DO ID for ataxia_and_polyneuropathy_adult_onset -> MT-ATP6 (SPMIT.07)
no DO ID for angioedema_induced_by_ace_inhibitors -> XPNPEP2 (SPAC22G7.01c)
no DO ID for striatonigral_degeneration_infantile_mitochondrial -> MT-ATP6 (SPMIT.07)
no DO ID for neural_tube_defects_folate_sensitive -> MTHFR (SPAC343.10)
no DO ID for microvascular_complications_of_diabetes_6 -> SOD2 (SPAC1486.01)
no DO ID for pulmonary_hypertension_neonatal -> CPS1 (SPBC215.08c)
no DO ID for polysubstance_abuse -> FAAH (SPCC550.07)
no DO ID for autism_16 -> SLC9A9 (SPAC15A10.06)
no DO ID for skin_hair_eye_pigmentation_variation_in_5 -> SLC45A2 (SPAC2F3.08)
no DO ID for uric_acid_concentration_serum_quantitative_trait_locus_4 -> SLC17A3 (SPAC1002.16c)
no DO ID for neural_tube_defects_folate_sensitive -> MTR (SPAC57A7.07c)
no DO ID for melanoma_cutaneous_malignant_9_2 -> TERT (SPBC29A3.14c)
no DO ID for diabetes_mellitus_insulin_dependent_5 -> SUMO4 (SPBC365.06)
no DO ID for autism_19 -> EIF4E (SPBC1709.18)
no DO ID for neural_tube_defects_folate_sensitive -> MTRR (SPBC12C2.03c)
no DO ID for alcohol_sensitivity_acute -> ALDH2 (SPAC922.07c)
no DO ID for deafness_aminoglycoside_induced -> TRMU (SPAC23H4.04)
no DO ID for encephalopathy_acute_infection_induced_1 -> UNC93B1 (SPAC6F6.04c)
no DO ID for low_density_lipoprotein_cholesterol_level_quantitative_trait_locus_6 -> SORT1 (SPBC16C6.06)
no DO ID for blood_group_wright_antigen -> SLC4A1 (SPBC543.05c)
no DO ID for glycerol_quantitative_trait_locus -> AQP7 (SPAC977.17)
no DO ID for blood_group_swann_system -> SLC4A1 (SPBC543.05c)
no DO ID for blood_group_diego_system_2 -> SLC4A1 (SPBC543.05c)
no DO ID for glioma_susceptibility_1 -> IDH1 (SPAC6G10.08)
no DO ID for ige_responsiveness_atopic -> PLA2G7 (SPBC106.11c)
no DO ID for vacterl_association_with_hydrocephalus -> PTEN (SPBC609.02)
no DO ID for cowden_syndrome_2 -> SDHB (SPAC140.01)
no DO ID for paroxysmal_nocturnal_hemoglobinuria_2 -> PIGT (SPBC1604.15)
no DO ID for gastric_cancer_hereditary_diffuse -> KRAS (SPAC17H9.09c)
no DO ID for cardiac_conduction_defect -> AKAP10 (SPAC23G3.05c)
no DO ID for thrombophilia_due_to_thrombin_defect -> MTHFR (SPAC343.10)
no DO ID for epilepsy_juvenile_myoclonic_10 -> ICK (SPAC3C7.06c)
no DO ID for impdh2_enzyme_activity_variation_in -> IMPDH2 (SPBC2F12.14c)
no DO ID for aniridia_2 -> ELP4 (SPCC11E10.06c)
no DO ID for homocystinuria_due_to_cbs_deficiency -> CBS (SPBC36.04)
no DO ID for charcot_marie_tooth_disease_type_2f -> HSPB1 (SPCC338.06c)
no DO ID for lynch_syndrome_i -> MLH1 (SPBC1703.04)
no DO ID for mutyh_associated_polyposis -> MUTYH (SPAC26A3.02)
no DO ID for familial_porphyria_cutanea_tarda -> UROD (SPCC4B3.05c)
no DO ID for blood_group_langereis_system -> ABCB6 (SPCC737.09c)
no DO ID for melanocytic_nevus_syndrome_congenital -> HRAS (SPAC17H9.09c)
no DO ID for spastic_paraplegia_13 -> HSPD1 (SPAC12G12.04)
no DO ID for spastic_paraplegia_12 -> RTN2 (SPBC31A8.01c)
no DO ID for spastic_paraplegia_17 -> BSCL2 (SPAC3A11.04)
no DO ID for pyridoxal_5_phosphate_dependent_epilepsy -> PNPO (SPAC1093.02)
no DO ID for inclusion_body_myopathy_with_early_onset_paget_disease_and_frontotemporal_dementia -> VCP (SPAC1565.08)
no DO ID for gnao1_encephalopathy -> GNAO1 (SPBC24C6.06)
no DO ID for dyskeratosis_congenita_autosomal_dominant -> TERT (SPBC29A3.14c)
no DO ID for cerebro_oculo_facio_skeletal_syndrome_cofs -> ERCC6 (SPCP25A2.02c)
no DO ID for north_american_indian_childhood_cirrhosis -> UTP4 (SPBC19F5.02c)
no DO ID for aplasia_cutis_congenita -> BMS1 (SPBC31E1.06)
no DO ID for pyogenic_arthritis_pyoderma_gangrenosum_and_acne -> PSTPIP1 (SPBC11C11.02)
no DO ID for hypochromic_microcytic_anemia_with_iron_overload -> SLC11A2 (SPAC27F1.08)
no DO ID for spastic_paraplegia_39 -> PNPLA6 (SPCC4B3.04c)
no DO ID for spastic_paraplegia_9 -> ALDH18A1 (SPAC17H9.13c)
no DO ID for chromosome_xq28_deletion_syndrome -> BCAP31 (SPAC9E9.04)
no DO ID for nakajo_syndrome -> PSMB8 (SPAC4A8.13c)
no DO ID for leukonychia_totalis -> PLCD1 (SPAC22F8.11)
no DO ID for alg1_congenital_disorder_of_glycosylation -> ALG1 (SPAC23C4.14)
no DO ID for congenital_disorder_of_glycosylation_type_ie -> PMM2 (SPAC1556.07)
no DO ID for giant_congenital_nevus -> NRAS (SPAC17H9.09c)
no DO ID for stxbp1_encephalopathy_with_epilepsy -> STXBP1 (SPCC584.05)
no DO ID for dicer1_related_pleuropulmonary_blastoma_cancer_predisposition_syndrome -> DICER1 (SPCC188.13c)
no DO ID for paroxysmal_choreoathetosis -> PNKD (SPAC824.07)
no DO ID for alg12_congenital_disorder_of_glycosylation -> ALG12 (SPBC1734.12c)
no DO ID for combined_oxidative_phosphorylation_deficiency_35 -> TRIT1 (SPAC343.15)
no DO ID for duane_syndrome_type_2 -> CHN1 (SPBC23G7.08c)
no DO ID for neurodevelopmental_disorder_with_microcephaly_seizures_and_cortical_atrophy -> VARS (SPAC4A8.08c)
no DO ID for spondyloepimetaphyseal_dysplasia_with_multiple_dislocations -> KIF22 (SPBC1604.20c)
no DO ID for deafness_autosomal_dominant_nonsyndromic_sensorineural_17 -> MYH9 (SPCC645.05c)
no DO ID for fitzsimmons_guilbert_syndrome -> TBL1XR1 (SPCC1235.09)
no DO ID for nsdhl_related_disorders -> NSDHL (SPBC3F6.02c)
no DO ID for stomatocytosis_i -> RHAG (SPAC2E1P3.02c)
no DO ID for macrozoospermia -> AURKC (SPCC320.13c)
no DO ID for cataract_hutterite_type -> LEMD2 (SPAC18G6.10)
no DO ID for polycystic_liver_disease_1_with_or_without_kidney_cysts -> SEC63 (SPBC36B7.03)
no DO ID for zellweger_spectrum_disorder -> PEX6 (SPAC17A5.01)
no DO ID for glioblastoma -> PTEN (SPBC609.02)
no DO ID for anemia_sideroblastic_2_pyridoxine_refractory -> GLRX5 (SPAPB2B4.02)
no DO ID for diamond_blackfan_anemia_1 -> RPL5 (SPBC11C11.09c)
no DO ID for lactose_intolerance_adult_type -> MCM6 (SPBC211.04c)
no DO ID for pseudohyperkalemia_familial_2_due_to_red_cell_leak -> SLC4A1 (SPBC543.05c)
no DO ID for rrm2b_related_mitochondrial_dna_depletion_syndrome -> RRM2B (SPBC25D12.04)
no DO ID for saccharopinuria -> AASS (SPAC227.18)
no DO ID for zellweger_spectrum_disorder -> PEX12 (SPAPB17E12.03)
no DO ID for familial_acute_necrotizing_encephalopathy -> RANBP2 (SPBC1773.07c)
no DO ID for glioblastoma -> MTOR (SPBC30D10.10c)
no DO ID for carney_triad -> SDHC (SPCC330.12c)
no DO ID for dysferlinopathy -> DYSF (SPAC1296.04)
no DO ID for mitochondrial_disorders -> POLG (SPCC24B10.22)
no DO ID for t_cell_prolymphocytic_leukemia -> ATM (SPCC23B6.03c)
no DO ID for schindler_disease -> NAGA (SPAC869.07c)
no DO ID for glioblastoma -> NRAS (SPAC17H9.09c)
no DO ID for atrial_standstill_1 -> MYH7 (SPCC645.05c)
no DO ID for auriculocondylar_syndrome_1 -> PLCB4 (SPAC22F8.11)
no DO ID for mbd5_haploinsufficiency -> MBD5 (SPBC21C3.14c)
no DO ID for cerebro_oculo_facio_skeletal_syndrome_cofs -> ERCC2 (SPAC1D4.12)
no DO ID for glioblastoma -> HRAS (SPAC17H9.09c)
no DO ID for multiple_mitochondrial_dysfunctions_syndrome -> ISCA1 (SPCC645.03c)
no DO ID for carney_triad -> SDHB (SPAC140.01)
no DO ID for mitochondrial_disorders -> MT-ATP6 (SPMIT.07)
no DO ID for acquired_idiopathic_sideroblastic_anemia -> MT-CO1 (SPMIT.01)
no DO ID for mitochondrial_disorders -> SLC25A4 (SPBC530.10c)
no DO ID for monogenic_diabetes -> GCK (SPAC4F8.07c)
no DO ID for spastic_paraparesis -> SPAST (SPAC328.04)
no DO ID for hyper_ige_syndrome_2 -> PGM3 (SPAC13C5.05c)
no DO ID for carney_triad -> SDHA (SPAC1556.02c)
no DO ID for proteus_like_syndrome -> PTEN (SPBC609.02)
no DO ID for ceroid_storage_disease -> PPT1 (SPBC530.12c)
no DO ID for myopathy_congenital_with_fiber_type_disproportion -> MYH7 (SPCC645.05c)
no DO ID for splenomegaly -> SBDS (SPBC21C3.19)
no DO ID for zellweger_spectrum_disorder -> PEX1 (SPCC553.03)
no DO ID for congenital_heart_defects_hamartomas_of_tongue_and_polysyndactyly -> TSC1 (SPAC22F3.13)
no DO ID for congenital_heart_defects_hamartomas_of_tongue_and_polysyndactyly -> TSC2 (SPAC18B11.11)
no DO ID for human_venous_malformation -> GLMN (SPAC15F9.01c)
no DO ID for rrm2b_related_mitochondrial_disease -> RRM2B (SPBC25D12.04)
no DO ID for deafness_autosomal_recessive -> OTOF (SPAC1296.04)
no DO ID for lynch_syndrome_i -> PMS2 (SPAC19G12.02c)
no DO ID for lynch_syndrome_i -> MSH6 (SPCC285.16c)
no DO ID for diamond_blackfan_anemia_15_with_mandibulofacial_dysostosis_2 -> RPS26 (SPAC1805.11c)
no DO ID for myoclonic_epilepsy_myopathy_sensory_ataxia -> POLG (SPCC24B10.22)
no DO ID for chronic_intestinal_pseudoobstruction -> ACTG2 (SPBC32H8.12c)
no DO ID for diamond_blackfan_anemia_15_with_mandibulofacial_dysostosis_2 -> TSR2 (SPBC409.15)
no DO ID for autosomal_recessive_non_syndromic_sensorineural_deafness_type_dfnb -> MYH9 (SPCC645.05c)
no DO ID for atrial_standstill_1 -> TTR (SPCC285.04)
no DO ID for cornelia_de_lange_syndrome_1 -> TAF6 (SPCC16C4.18c)
no DO ID for aortic_aneurysm_familial_thoracic_2 -> ACTA2 (SPBC32H8.12c)
no DO ID for zimmermann_laband_syndrome_1 -> ATP6V1B2 (SPAC637.05c)
no DO ID for familial_colorectal_cancer -> MT-CO2 (SPMIT.11)
no DO ID for myh9_related_thrombocytopenia -> MYH9 (SPCC645.05c)
no DO ID for breast_ovarian_cancer_familial_1_2 -> NBN (SPBC6B1.09c)
no DO ID for familial_colorectal_cancer -> MT-CO1 (SPMIT.01)
no DO ID for hereditary_hearing_loss_and_deafness -> SF3B4 (SPAC31G5.01)
no DO ID for nicolaides_baraitser_syndrome_2 -> ARID1B (SPBC30B4.04c)
no DO ID for wiedemann_steiner_syndrome -> SMC3 (SPAC10F6.09c)
no DO ID for familial_colorectal_cancer -> MT-CYB (SPMIT.05)
no DO ID for polg_related_disorders -> POLG (SPCC24B10.22)
no DO ID for myoglobinuria_recurrent_2 -> MT-CO1 (SPMIT.01)
no DO ID for seizure_disorder -> PNPO (SPAC1093.02)
no DO ID for glutathionuria -> GGT1 (SPAC664.09)
no DO ID for hypertelorism -> MT-ATP6 (SPMIT.07)
no DO ID for mitochondrial_disorders -> TOP3A (SPBC16G5.12c)
no DO ID for mitochondrial_disorders -> MT-CO2 (SPMIT.11)
no DO ID for alacrima_achalasia_and_mental_retardation_syndrome -> KAT6A (SPAC17G8.13c)
no DO ID for alacrima_achalasia_and_mental_retardation_syndrome -> OTUD6B (SPAC1952.03)
no DO ID for alacrima_achalasia_and_mental_retardation_syndrome -> PHF8 (SPCC622.16c)
no DO ID for alacrima_achalasia_and_mental_retardation_syndrome -> MED12 (SPAC688.08)
no DO ID for alacrima_achalasia_and_mental_retardation_syndrome -> KDM5C (SPAC343.11c)
no DO ID for alacrima_achalasia_and_mental_retardation_syndrome -> SLC16A2 (SPAC2G11.13)
no DO ID for alacrima_achalasia_and_mental_retardation_syndrome -> BRPF1 (SPBC17D11.04c)
no DO ID for alacrima_achalasia_and_mental_retardation_syndrome -> ATP2B3 (SPAPB2B4.04c)
no DO ID for alacrima_achalasia_and_mental_retardation_syndrome -> CUL4B (SPAC3A11.08)
no DO ID for alacrima_achalasia_and_mental_retardation_syndrome -> GNB1 (SPBC32H8.07)
no DO ID for alacrima_achalasia_and_mental_retardation_syndrome -> DYRK1A (SPAC823.03)
no DO ID for amaurosis_congenita_cone_rod_type_with_congenital_hypertrichosis_2 -> CNNM4 (SPCC4B3.03c)
no DO ID for anemia_sideroblastic_3_pyridoxine_refractory -> SLC25A38 (SPAC823.10c)
no DO ID for ataxia_and_polyneuropathy_adult_onset -> ATM (SPCC23B6.03c)
no DO ID for ataxia_and_polyneuropathy_adult_onset -> SETX (SPAC6G9.10c)
no DO ID for atp6v0a2_related_cutis_laxa -> ATP6V0A2 (SPAC16E8.07c)
no DO ID for atrial_standstill_1 -> ACTN2 (SPAC15A10.08)
no DO ID for atrial_standstill_1 -> MIPEP (SPAC1F3.10c)
no DO ID for bap1_tumor_predisposition_syndrome -> PMS2 (SPAC19G12.02c)
no DO ID for camptodactyly_1 -> MT-ATP6 (SPMIT.07)
no DO ID for cerebellar_atrophy_developmental_delay_and_seizures -> BRPF1 (SPBC17D11.04c)
no DO ID for cerebral_visual_impairment -> GNB1 (SPBC32H8.07)
no DO ID for cerebrooculofacioskeletal_syndrome_1 -> ERCC2 (SPAC1D4.12)
no DO ID for ceroid_storage_disease -> DNAJC5 (SPBC11B10.05c)
no DO ID for ceroid_storage_disease -> CLN3 (SPAC607.09c)
no DO ID for combined_oxidative_phosphorylation_deficiency_1 -> NARS2 (SPBC1198.10c)
no DO ID for corpus_callosum_agenesis_of -> MED12 (SPAC688.08)
no DO ID for corpus_callosum_agenesis_of -> ARID1B (SPBC30B4.04c)
no DO ID for distal_hereditary_motor_neuropathies -> IGHMBP2 (SPCC737.07c)
no DO ID for heart_valve_disease -> SMC1A (SPBC29A10.04)
no DO ID for hypertonia -> SMC1A (SPBC29A10.04)
no DO ID for inherited_bone_marrow_failure_syndromes -> DNAJC21 (SPAC6B12.08)
no DO ID for interatrial_communication -> RPL5 (SPBC11C11.09c)
no DO ID for leukemia_acute_lymphoblastic -> GNB1 (SPBC32H8.07)
no DO ID for macrocephaly_megalencephaly_syndrome_autosomal_recessive -> STXBP1 (SPCC584.05)
no DO ID for macrocephaly_megalencephaly_syndrome_autosomal_recessive -> RPS6KA3 (SPCC4G3.08)
no DO ID for mitochondrial_disorders -> RMND1 (SPCC16C4.01)
no DO ID for mitochondrial_disorders -> RRM2B (SPBC25D12.04)
no DO ID for mitochondrial_disorders -> YARS2 (SPCC576.06c)
no DO ID for mitochondrial_disorders -> GFM2 (SPBC660.10)
no DO ID for mitochondrial_disorders -> ATP5F1D (SPBC13E7.04)
no DO ID for mitochondrial_disorders -> GFER (SPBC146.04)
no DO ID for neuronal_migration_disorders -> DYNC1H1 (SPAC1093.06c)
no DO ID for neutropenia_severe_congenital_1_autosomal_dominant_2 -> TCIRG1 (SPAC16E8.07c)
no DO ID for non_syndromic_genetic_deafness -> KARS (SPCC18.08)
no DO ID for non_syndromic_genetic_deafness -> MYH9 (SPCC645.05c)
no DO ID for non_syndromic_genetic_deafness -> OTOF (SPAC1296.04)
no DO ID for parkinson_disease_10 -> VPS13C (SPBC21C3.01c)
no DO ID for peroxisome_biogenesis_disorder_1a -> PEX10 (SPBC17A3.10)
no DO ID for polyglucosan_body_myopathy_1_with_or_without_immunodeficiency -> SURF1 (SPBC1215.01)
no DO ID for porphyria_cutanea_tarda_type_i -> UROD (SPCC4B3.05c)
no DO ID for pseudohypoaldosteronism_type_iia -> CUL3 (SPAC24H6.03)
no DO ID for pulmonary_hypertension_primary_1 -> RPL5 (SPBC11C11.09c)
no DO ID for rare_adenocarcinoma_of_the_breast -> RB1CC1 (SPAC7D4.04)
no DO ID for rare_adenocarcinoma_of_the_breast -> KRAS (SPAC17H9.09c)
no DO ID for scoliosis_isolated_1 -> MAPK7 (SPBC119.08)
no DO ID for segawa_syndrome_autosomal_recessive -> GCH1 (SPAC17A5.13)
no DO ID for seizure_disorder -> WDR45 (SPAC458.06)
no DO ID for seizure_disorder -> MYO5A (SPCC1919.10c)
no DO ID for seizure_disorder -> NALCN (SPAC6F6.01)
no DO ID for seizure_disorder -> OTUD6B (SPAC1952.03)
no DO ID for seizure_disorder -> GSPT2 (SPCC584.04)
no DO ID for seizure_disorder -> DYRK1A (SPAC823.03)
no DO ID for seizure_disorder -> GNB1 (SPBC32H8.07)
no DO ID for seizure_disorder -> TSC1 (SPAC22F3.13)
no DO ID for seizure_disorder -> STXBP1 (SPCC584.05)
no DO ID for seizure_disorder -> SPAST (SPAC328.04)
no DO ID for seizure_disorder -> SCO2 (SPBC119.06)
no DO ID for seizure_disorder -> ARFGEF2 (SPAC4D7.01c)
no DO ID for seizure_disorder -> CUL4B (SPAC3A11.08)
no DO ID for specific_granule_deficiency_1 -> SMARCD2 (SPAC23G3.10c)
no DO ID for spermatogenic_failure_1 -> PDHA2 (SPAC26F1.03)
no DO ID for talipes_equinovarus -> DARS2 (SPCC736.06)
no DO ID for trichomegaly -> ARID1B (SPBC30B4.04c)
no DO ID for tumor_predisposition_syndrome -> PMS2 (SPAC19G12.02c)
no DO ID for yemenite_deaf_blind_hypopigmentation_syndrome -> PMPCA (SPBC18E5.12c)
no DO ID for zellweger_spectrum_disorder -> PEX10 (SPBC17A3.10)
no DO ID for neonatal_adrenoleukodystrophy -> PEX1 (SPCC553.03)
no DO ID for amelogenesis_imperfecta_hypomaturation_type -> WDR72 (SPBC16H5.13)
no DO ID for neonatal_adrenoleukodystrophy -> PEX10 (SPBC17A3.10)
no DO ID for autosomal_dominant_progressive_external_ophthalmoplegia -> RRM2B (SPBC25D12.04)
no DO ID for zimmermann_laband_syndrome -> ATP6V1B2 (SPAC637.05c)
no DO ID for neonatal_adrenoleukodystrophy -> PEX6 (SPAC17A5.01)
no DO ID for cap_myopathy -> TPM3 (SPAC27F1.02c)
no DO ID for muscle_eye_brain_disease_2 -> POMT1 (SPBC16C6.09)
no DO ID for autosomal_dominant_progressive_external_ophthalmoplegia -> POLG (SPCC24B10.22)
no DO ID for autosomal_dominant_progressive_external_ophthalmoplegia -> SLC25A4 (SPBC530.10c)
no DO ID for chronic_eosinophilic_leukemia -> FIP1L1 (SPAC22G7.10)
no DO ID for juvenile_amyotrophic_lateral_sclerosis -> SIGMAR1 (SPAC20G8.07c)
no DO ID for oculoectodermal_syndrome -> KRAS (SPAC17H9.09c)
no DO ID for alport_syndrome_intellectual_disability_midface_hypoplasia_elliptocytosis_syndrome -> AMMECR1 (SPAC688.03c)
no DO ID for hyperphosphatasia_intellectual_disability_syndrome -> PIGV (SPAC18B11.05)
no DO ID for hyperphosphatasia_intellectual_disability_syndrome -> PIGO (SPBC27B12.06)
no DO ID for precursor_t_cell_acute_lymphoblastic_leukemia -> PICALM (SPBC19F8.03c)
no DO ID for autosomal_dominant_macrothrombocytopenia -> TUBB1 (SPBC26H8.07c)
no DO ID for distal_hereditary_motor_neuropathy_type_ii -> HSPB8 (SPCC338.06c)
no DO ID for neonatal_adrenoleukodystrophy -> PEX12 (SPAPB17E12.03)
no DO ID for neonatal_adrenoleukodystrophy -> PEX13 (SPAC3C7.10)
no DO ID for acute_myeloid_leukemia_with_t816p11p13_translocation -> KAT6A (SPAC17G8.13c)
no DO ID for muscle_eye_brain_disease_2 -> B3GALNT2 (SPBC1921.06c)
no DO ID for muscle_eye_brain_disease_2 -> POMT2 (SPAC22A12.07c)
no DO ID for muscle_eye_brain_disease_2 -> GMPPB (SPCC1906.01)
no DO ID for gordon_holmes_syndrome -> PNPLA6 (SPCC4B3.04c)
no DO ID for pontocerebellar_hypoplasia_type_1 -> EXOSC3 (SPAC22A12.12c)
no DO ID for neonatal_adrenoleukodystrophy -> PEX16 (SPBC646.15c)
no DO ID for neonatal_adrenoleukodystrophy -> PEX19 (SPAC17C9.14)
no DO ID for neonatal_adrenoleukodystrophy -> PEX14 (SPBC13G1.03c)
no DO ID for neonatal_adrenoleukodystrophy -> PEX3 (SPAC29A4.14c)
no DO ID for geroderma_osteodysplasticum -> PYCR1 (SPAPYUG7.05)
no DO ID for ferro_cerebro_cutaneous_syndrome -> PIGA (SPBC3D6.07)
no DO ID for distal_hereditary_motor_neuropathy_type_v_2 -> REEP1 (SPBC30D10.09c)
no DO ID for auriculo_condylar_syndrome -> PLCB4 (SPAC22F8.11)
no DO ID for severe_congenital_nemaline_myopathy -> NEB (SPAC9G1.06c)
no DO ID for pontocerebellar_hypoplasia_type_1 -> TSEN54 (SPCC613.09)
no DO ID for autosomal_recessive_malignant_osteopetrosis -> TCIRG1 (SPAC16E8.07c)
no DO ID for homozygous_familial_hypercholesterolemia -> PCSK9 (SPAC1006.01)
no DO ID for cataract_microcornea_syndrome -> CRYAA (SPCC338.06c)
no DO ID for zebra_body_myopathy -> ACTA1 (SPBC32H8.12c)
no DO ID for autosomal_dominant_macrothrombocytopenia -> ACTN1 (SPAC15A10.08)
no DO ID for fryns_syndrome -> PIGN (SPBC839.08c)
no DO ID for hypotrichosis_simplex -> RPL21 (SPAC959.08)
no DO ID for hypotrichosis_simplex -> SNRPE (SPBC11G11.06c)
no DO ID for glycosylphosphatidylinositol_deficiency -> PIGW (SPAC144.10c)
no DO ID for precursor_t_cell_acute_lymphoblastic_leukemia -> NUP214 (SPAC23D3.06c)
no DO ID for 46xx_sex_reversal_1_2 -> PSMC3IP (SPAC222.15)
no DO ID for 46xx_sex_reversal_1_2 -> NUP107 (SPBC428.01c)
no DO ID for acquired_idiopathic_sideroblastic_anemia -> SF3B1 (SPAC27F1.09c)
no DO ID for acrocephalopolydactylous_dysplasia -> MYO5A (SPCC1919.10c)
no DO ID for acute_myeloid_leukemia_with_abnormal_bone_marrow_eosinophils_inv16p13q22_or_t1616p13q22 -> MYH11 (SPCC645.05c)
no DO ID for acute_myeloid_leukemia_with_inv3p21q262_or_t33p21q262 -> RPN1 (SPAC27F1.07)
no DO ID for acute_myeloid_leukemia_with_t69p23q34 -> NUP214 (SPAC23D3.06c)
no DO ID for acute_myeloid_leukemia_with_t911p22q23 -> MLLT3 (SPAC17G8.07)
no DO ID for acute_neonatal_citrullinemia_type_i -> ASS1 (SPBC428.05c)
no DO ID for adenosine_monophosphate_deaminase_1_deficiency -> AMPD3 (SPBC106.04)
no DO ID for adrenal_hyperplasia_congenital_due_to_17_alpha_hydroxylase_deficiency -> CYB5A (SPCC16A11.10c)
no DO ID for adult_onset_citrullinemia_type_i -> ASS1 (SPBC428.05c)
no DO ID for adult_onset_distal_myopathy_due_to_vcp_mutation -> VCP (SPAC1565.08)
no DO ID for anemia_congenital_dyserythropoietic_type_iii -> KIF23 (SPBC15D4.01c)
no DO ID for angioma_tufted -> GNA14 (SPBC24C6.06)
no DO ID for arthrogryposis_distal_type_2a -> NALCN (SPAC6F6.01)
no DO ID for arthrogryposis_distal_type_5 -> NALCN (SPAC6F6.01)
no DO ID for athyreosis -> SLC26A4 (SPBC3H7.02)
no DO ID for atypical_juvenile_parkinsonism -> SYNJ1 (SPBC2G2.02)
no DO ID for autoimmune_hemolytic_anemia_autoimmune_thrombocytopenia_primary_immunodeficiency_syndrome -> TPP2 (SPAP8A3.12c)
no DO ID for autosomal_dominant_charcot_marie_tooth_disease_type_2_due_to_dgat2_mutation -> DGAT2 (SPCC1235.15)
no DO ID for autosomal_dominant_complex_spastic_paraplegia_type_9b -> ALDH18A1 (SPAC17H9.13c)
no DO ID for autosomal_dominant_distal_axonal_motor_neuropathy_myofibrillar_myopathy_syndrome -> HSPB8 (SPCC338.06c)
no DO ID for autosomal_dominant_epilepsy_with_auditory_features -> DEPDC5 (SPBC26H8.04c)
no DO ID for autosomal_dominant_macrothrombocytopenia -> TPM4 (SPAC27F1.02c)
no DO ID for autosomal_dominant_non_syndromic_sensorineural_deafness_type_dfna -> OSBPL2 (SPBC2F12.05c)
no DO ID for autosomal_dominant_non_syndromic_sensorineural_deafness_type_dfna -> MYH14 (SPCC645.05c)
no DO ID for autosomal_dominant_non_syndromic_sensorineural_deafness_type_dfna -> MYH9 (SPCC645.05c)
no DO ID for autosomal_dominant_non_syndromic_sensorineural_deafness_type_dfna -> SLC17A8 (SPAC1002.16c)
no DO ID for autosomal_dominant_non_syndromic_sensorineural_deafness_type_dfna -> ACTG1 (SPBC32H8.12c)
no DO ID for autosomal_dominant_non_syndromic_sensorineural_deafness_type_dfna -> MCM2 (SPBC4.04c)
no DO ID for autosomal_dominant_non_syndromic_sensorineural_deafness_type_dfna -> CRYM (SPAP11E10.01)
no DO ID for autosomal_dominant_non_syndromic_sensorineural_deafness_type_dfna -> DIAPH3 (SPCC895.05)
no DO ID for autosomal_dominant_non_syndromic_sensorineural_deafness_type_dfna -> DMXL2 (SPBC1105.10)
no DO ID for autosomal_recessive_ataxia_due_to_pex10_deficiency -> PEX10 (SPBC17A3.10)
no DO ID for autosomal_recessive_chorioretinopathy_microcephaly_syndrome -> TUBGCP4 (SPBC211.06)
no DO ID for autosomal_recessive_isolated_optic_atrophy -> RTN4IP1 (SPBC16A3.02c)
no DO ID for autosomal_recessive_isolated_optic_atrophy -> ACO2 (SPAC24C9.06c)
no DO ID for autosomal_recessive_malignant_osteopetrosis -> CLCN7 (SPBC887.02)
no DO ID for autosomal_recessive_non_syndromic_sensorineural_deafness_type_dfnb -> OTOF (SPAC1296.04)
no DO ID for autosomal_recessive_non_syndromic_sensorineural_deafness_type_dfnb -> WBP2 (SPAC29B12.11c)
no DO ID for autosomal_recessive_non_syndromic_sensorineural_deafness_type_dfnb -> SYNE4 (SPBC947.12)
no DO ID for autosomal_recessive_non_syndromic_sensorineural_deafness_type_dfnb -> SLC26A5 (SPBC3H7.02)
no DO ID for autosomal_recessive_non_syndromic_sensorineural_deafness_type_dfnb -> MSRB3 (SPBC216.04c)
no DO ID for autosomal_recessive_non_syndromic_sensorineural_deafness_type_dfnb -> BDP1 (SPCC1919.14c)
no DO ID for autosomal_recessive_non_syndromic_sensorineural_deafness_type_dfnb -> CDC14A (SPAC1782.09c)
no DO ID for autosomal_recessive_non_syndromic_sensorineural_deafness_type_dfnb -> KARS (SPCC18.08)
no DO ID for autosomal_recessive_sideroblastic_anemia -> SLC25A38 (SPAC823.10c)
no DO ID for autosomal_recessive_sideroblastic_anemia -> HSPA9 (SPAC664.11)
no DO ID for autosomal_recessive_spastic_paraplegia_type_59 -> USP8 (SPBC18H10.08c)
no DO ID for autosomal_recessive_spastic_paraplegia_type_60 -> WDR48 (SPAC31A2.14)
no DO ID for autosomal_recessive_spastic_paraplegia_type_66 -> ARSI (SPBPB10D8.02c)
no DO ID for autosomal_recessive_spastic_paraplegia_type_67 -> PGAP1 (SPAC824.02)
no DO ID for autosomal_recessive_spastic_paraplegia_type_70 -> MARS (SPBC17A3.04c)
no DO ID for autosomal_thrombocytopenia_with_normal_platelets -> MASTL (SPAPB18E9.02c)
no DO ID for autosomal_thrombocytopenia_with_normal_platelets -> CYCS (SPCC191.07)
no DO ID for basal_ganglia_calcification_idiopathic_1 -> XPR1 (SPAC227.01c)
no DO ID for cerebellar_ataxia_mental_retardation_and_dysequilibrium_syndrome_1 -> TUBB2B (SPBC26H8.07c)
no DO ID for cerebellar_ataxia_mental_retardation_and_dysequilibrium_syndrome_1 -> ATP8A2 (SPBC887.12)
no DO ID for childhood_onset_nemaline_myopathy -> TPM3 (SPAC27F1.02c)
no DO ID for childhood_onset_nemaline_myopathy -> NEB (SPAC9G1.06c)
no DO ID for childhood_onset_nemaline_myopathy -> ACTA1 (SPBC32H8.12c)
no DO ID for cholestasis_progressive_familial_intrahepatic_1_2 -> MYO5B (SPCC1919.10c)
no DO ID for clcn4_related_x_linked_intellectual_disability_syndrome -> CLCN4 (SPBC887.02)
no DO ID for cockayne_syndrome_type_i -> ERCC6 (SPCP25A2.02c)
no DO ID for cockayne_syndrome_type_i -> ERCC4 (SPCC970.01)
no DO ID for cockayne_syndrome_type_ii -> ERCC8 (SPBC577.09)
no DO ID for cockayne_syndrome_type_ii -> ERCC1 (SPBC4F6.15c)
no DO ID for cockayne_syndrome_type_iii -> ERCC8 (SPBC577.09)
no DO ID for cockayne_syndrome_type_iii -> ERCC6 (SPCP25A2.02c)
no DO ID for coloboma_of_eye_lens -> ABCB6 (SPCC737.09c)
no DO ID for coloboma_of_eyelid -> ABCB6 (SPCC737.09c)
no DO ID for coloboma_ocular_autosomal_dominant -> ABCB6 (SPCC737.09c)
no DO ID for coloboma_ocular_autosomal_dominant -> ACTG1 (SPBC32H8.12c)
no DO ID for colobomatous_microphthalmia -> ABCB6 (SPCC737.09c)
no DO ID for combined_oxidative_phosphorylation_deficiency_19 -> NFS1 (SPBC21D10.11c)
no DO ID for complete_atrioventricular_canal_ventricle_hypoplasia_syndrome -> GATA6 (SPCC1902.01)
no DO ID for congenital_cataract_hypertrophic_cardiomyopathy_mitochondrial_myopathy_syndrome -> SLC25A4 (SPBC530.10c)
no DO ID for congenital_generalized_hypercontractile_muscle_stiffness_syndrome -> TPM3 (SPAC27F1.02c)
no DO ID for congenital_insensitivity_to_pain_with_severe_intellectual_disability -> CLTCL1 (SPAC26A3.05)
no DO ID for congenital_muscular_dystrophy_with_cerebellar_involvement -> POMT1 (SPBC16C6.09)
no DO ID for congenital_muscular_dystrophy_with_cerebellar_involvement -> POMT2 (SPAC22A12.07c)
no DO ID for congenital_muscular_dystrophy_with_cerebellar_involvement -> GMPPB (SPCC1906.01)
no DO ID for congenital_muscular_dystrophy_with_intellectual_disability -> POMT2 (SPAC22A12.07c)
no DO ID for congenital_muscular_dystrophy_with_intellectual_disability -> POMT1 (SPBC16C6.09)
no DO ID for congenital_muscular_dystrophy_with_intellectual_disability -> GMPPB (SPCC1906.01)
no DO ID for congenital_muscular_dystrophy_without_intellectual_disability -> POMT1 (SPBC16C6.09)
no DO ID for congenital_myasthenic_syndromes_with_glycosylation_defect -> GMPPB (SPCC1906.01)
no DO ID for congenital_myasthenic_syndromes_with_glycosylation_defect -> GFPT1 (SPBC12C2.11)
no DO ID for congenital_myasthenic_syndromes_with_glycosylation_defect -> DPAGT1 (SPBC15D4.04)
no DO ID for congenital_myasthenic_syndromes_with_glycosylation_defect -> ALG2 (SPBC11B10.01)
no DO ID for congenital_myasthenic_syndromes_with_glycosylation_defect -> ALG14 (SPAC5D6.06c)
no DO ID for congenital_myopathy_paradas_type -> DYSF (SPAC1296.04)
no DO ID for congenital_sucrase_isomaltase_deficiency_with_minimal_starch_tolerance -> SI (SPAC30D11.01c)
no DO ID for congenital_sucrase_isomaltase_deficiency_with_starch_and_lactose_intolerance -> SI (SPAC30D11.01c)
no DO ID for congenital_sucrase_isomaltase_deficiency_with_starch_intolerance -> SI (SPAC30D11.01c)
no DO ID for congenital_sucrase_isomaltase_deficiency_without_starch_intolerance -> SI (SPAC30D11.01c)
no DO ID for congenital_sucrase_isomaltase_deficiency_without_sucrose_intolerance -> SI (SPAC30D11.01c)
no DO ID for corpus_callosum_agenesis_of_with_facial_anomalies_and_robin_sequence -> DDX3X (SPCC1795.11)
no DO ID for cryptogenic_multifocal_ulcerous_stenosing_enteritis -> PLA2G4A (SPCC1450.09c)
no DO ID for cytosolic_phospholipase_a2_alpha_deficiency_associated_bleeding_disorder -> PLA2G4A (SPCC1450.09c)
no DO ID for deafness_enamel_hypoplasia_nail_defects -> PEX6 (SPAC17A5.01)
no DO ID for deafness_aminoglycoside_induced -> MT-CO1 (SPMIT.01)
no DO ID for dentin_dysplasia_type_i -> VPS4B (SPAC2G11.06)
no DO ID for differentiated_thyroid_carcinoma -> NRAS (SPAC17H9.09c)
no DO ID for differentiated_thyroid_carcinoma -> TPR (SPCC162.08c)
no DO ID for differentiated_thyroid_carcinoma -> EIF1AX (SPBC25H2.07)
no DO ID for differentiated_thyroid_carcinoma -> KRAS (SPAC17H9.09c)
no DO ID for differentiated_thyroid_carcinoma -> HRAS (SPAC17H9.09c)
no DO ID for digitotalar_dysmorphism -> MYH3 (SPCC645.05c)
no DO ID for digitotalar_dysmorphism -> NALCN (SPAC6F6.01)
no DO ID for distal_hereditary_motor_neuropathy_type_7 -> DCTN1 (SPAC27D7.13c)
no DO ID for distal_hereditary_motor_neuropathy_type_ii -> HSPB1 (SPCC338.06c)
no DO ID for distal_hereditary_motor_neuropathy_type_ii -> HSPB3 (SPCC338.06c)
no DO ID for early_onset_nuclear_cataract -> UNC45B (SPCC613.04c)
no DO ID for early_onset_nuclear_cataract -> CRYAB (SPCC338.06c)
no DO ID for early_onset_nuclear_cataract -> CRYAA (SPCC338.06c)
no DO ID for early_onset_posterior_subcapsular_cataract -> UNC45B (SPCC613.04c)
no DO ID for early_onset_posterior_subcapsular_cataract -> LEMD2 (SPAC18G6.10)
no DO ID for early_onset_posterior_subcapsular_cataract -> CHMP4B (SPAC1142.07c)
no DO ID for early_onset_autosomal_dominant_alzheimer_disease_2 -> SORL1 (SPBC16C6.06)
no DO ID for epilepsy_familial_focal_with_variable_foci_1_2 -> NPRL3 (SPBC543.04)
no DO ID for epilepsy_familial_focal_with_variable_foci_1_2 -> NPRL2 (SPAC23H3.03c)
no DO ID for epilepsy_pyridoxine_dependent -> SLC13A5 (SPBC3B8.04c)
no DO ID for epilepsy_pyridoxine_dependent -> PLPBP (SPAC644.09)
no DO ID for erythrocyte_galactose_epimerase_deficiency -> GALE (SPBPB2B2.12c)
no DO ID for familial_colorectal_cancer_type_x -> RPS20 (SPCC576.09)
no DO ID for familial_idiopathic_steroid_resistant_nephrotic_syndrome_with_diffuse_mesangial_sclerosis -> NUP93 (SPCC1620.11)
no DO ID for familial_idiopathic_steroid_resistant_nephrotic_syndrome_with_diffuse_mesangial_sclerosis -> ARHGDIA (SPAC6F12.06)
no DO ID for familial_infantile_bilateral_striatal_necrosis -> NUP62 (SPAC26A3.15c)
no DO ID for familial_infantile_bilateral_striatal_necrosis -> MT-ATP6 (SPMIT.07)
no DO ID for familial_infantile_bilateral_striatal_necrosis -> ADAR (SPBC16A3.06)
no DO ID for familial_isolated_dilated_cardiomyopathy -> SDHA (SPAC1556.02c)
no DO ID for familial_isolated_dilated_cardiomyopathy -> DOLK (SPCC63.10c)
no DO ID for familial_isolated_dilated_cardiomyopathy -> CRYAB (SPCC338.06c)
no DO ID for familial_isolated_dilated_cardiomyopathy -> ACTC1 (SPBC32H8.12c)
no DO ID for familial_isolated_dilated_cardiomyopathy -> ACTN2 (SPAC15A10.08)
no DO ID for familial_isolated_dilated_cardiomyopathy -> MYH6 (SPCC645.05c)
no DO ID for familial_isolated_dilated_cardiomyopathy -> MYH7 (SPCC645.05c)
no DO ID for familial_isolated_restrictive_cardiomyopathy -> KIF20A (SPBC15D4.01c)
no DO ID for familial_partial_lipodystrophy_due_to_akt2_mutations -> AKT2 (SPCC24B10.07)
no DO ID for fatal_infantile_cytochrome_c_oxidase_deficiency -> SCO1 (SPBC119.06)
no DO ID for fatal_infantile_cytochrome_c_oxidase_deficiency -> COX15 (SPAC22E12.10c)
no DO ID for fatal_infantile_cytochrome_c_oxidase_deficiency -> COA6 (SPBC24C6.13)
no DO ID for fatal_infantile_cytochrome_c_oxidase_deficiency -> COA5 (SPBC16A3.16)
no DO ID for fatal_infantile_hypertrophic_cardiomyopathy_due_to_mitochondrial_complex_i_deficiency -> NDUFAF1 (SPAC9E9.15)
no DO ID for female_infertility_due_to_oocyte_meiotic_arrest -> TUBB8 (SPBC26H8.07c)
no DO ID for generalized_galactose_epimerase_deficiency -> GALE (SPBPB2B2.12c)
no DO ID for genetic_recurrent_myoglobinuria -> MT-CO3 (SPMIT.04)
no DO ID for genetic_recurrent_myoglobinuria -> MT-CO1 (SPMIT.01)
no DO ID for genetic_recurrent_myoglobinuria -> LPIN1 (SPAC1952.13)
no DO ID for global_developmental_delay_lung_cysts_overgrowth_wilms_tumor_syndrome -> DICER1 (SPCC188.13c)
no DO ID for glycine_encephalopathy_with_normal_serum_glycine -> GLDC (SPAC13G6.06c)
no DO ID for glycine_encephalopathy_with_normal_serum_glycine -> AMT (SPAC31G5.14)
no DO ID for glycine_encephalopathy_with_normal_serum_glycine -> GCSH (SPBP19A11.01)
no DO ID for glycogen_storage_disease_due_to_acid_maltase_deficiency_infantile_onset -> GAA (SPAC30D11.01c)
no DO ID for glycogen_storage_disease_due_to_acid_maltase_deficiency_late_onset -> GAA (SPAC30D11.01c)
no DO ID for hemolytic_anemia_due_to_glutathione_reductase_deficiency -> GSR (SPBC17A3.07)
no DO ID for hereditary_late_onset_parkinson_disease -> VPS35 (SPCC777.13)
no DO ID for hereditary_motor_and_sensory_neuropathy_v -> MFN2 (SPBC1706.03)
no DO ID for hereditary_neuroendocrine_tumor_of_small_intestine -> IPMK (SPAC607.04)
no DO ID for hereditary_paraganglioma_pheochromocytoma_syndromes -> FH (SPCC18.18c)
no DO ID for hereditary_paraganglioma_pheochromocytoma_syndromes -> SDHA (SPAC1556.02c)
no DO ID for hereditary_paraganglioma_pheochromocytoma_syndromes -> MDH2 (SPCC306.08c)
no DO ID for heritable_pulmonary_arterial_hypertension -> EIF2AK4 (SPBC36B7.09)
no DO ID for htra1_related_autosomal_dominant_cerebral_small_vessel_disease -> HTRA1 (SPAC23G3.12c)
no DO ID for hyperandrogenism_due_to_cortisone_reductase_deficiency -> H6PD (SPCC794.01c)
no DO ID for hyperparathyroidism_3 -> CDC73 (SPBC17G9.02c)
no DO ID for hyperphosphatasia_intellectual_disability_syndrome -> PIGY (SPAC227.19c)
no DO ID for hyperphosphatasia_intellectual_disability_syndrome -> PIGW (SPAC144.10c)
no DO ID for hyperphosphatasia_intellectual_disability_syndrome -> PGAP3 (SPAC823.07)
no DO ID for hyperphosphatasia_intellectual_disability_syndrome -> PIGL (SPAPB2B4.01c)
no DO ID for hypothyroidism_congenital_nongoitrous_2 -> SLC26A4 (SPBC3H7.02)
no DO ID for hypotonia_speech_impairment_severe_cognitive_delay_syndrome -> NALCN (SPAC6F6.01)
no DO ID for idiopathic_ventricular_fibrillation_non_brugada_type -> DPP6 (SPACUNK4.08)
no DO ID for immunodeficiency_14 -> PTEN (SPBC609.02)
no DO ID for infantile_glycine_encephalopathy -> GLDC (SPAC13G6.06c)
no DO ID for infantile_glycine_encephalopathy -> GCSH (SPBP19A11.01)
no DO ID for infantile_glycine_encephalopathy -> AMT (SPAC31G5.14)
no DO ID for inherited_congenital_spastic_tetraplegia -> ADD3 (SPBC359.06)
no DO ID for intellectual_disability_syndrome_due_to_a_dyrk1a_point_mutation -> DYRK1A (SPAC823.03)
no DO ID for intellectual_disability_obesity_brain_malformations_facial_dysmorphism_syndrome -> TRAPPC9 (SPAC6G10.05c)
no DO ID for intermediate_congenital_nemaline_myopathy -> TPM3 (SPAC27F1.02c)
no DO ID for intermediate_congenital_nemaline_myopathy -> NEB (SPAC9G1.06c)
no DO ID for intermediate_congenital_nemaline_myopathy -> ACTA1 (SPBC32H8.12c)
no DO ID for intermediate_severe_salla_disease -> SLC17A5 (SPAC1002.16c)
no DO ID for isolated_atp_synthase_deficiency -> MT-ATP8 (SPMIT.09)
no DO ID for isolated_atp_synthase_deficiency -> MT-ATP6 (SPMIT.07)
no DO ID for isolated_atp_synthase_deficiency -> ATPAF2 (SPAC9.12c)
no DO ID for isolated_atp_synthase_deficiency -> ATP5F1A (SPAC14C4.14)
no DO ID for isolated_complex_iii_deficiency -> UQCC3 (SPBC27B12.14)
no DO ID for isolated_complex_iii_deficiency -> UQCRB (SPCC737.02c)
no DO ID for isolated_complex_iii_deficiency -> UQCRC2 (SPCC613.10)
no DO ID for isolated_complex_iii_deficiency -> UQCRQ (SPAC1782.07)
no DO ID for isolated_complex_iii_deficiency -> CYC1 (SPBC29A3.18)
no DO ID for isolated_complex_iii_deficiency -> LYRM7 (SPBC30D10.21)
no DO ID for isolated_complex_iii_deficiency -> MT-CYB (SPMIT.05)
no DO ID for isolated_complex_iii_deficiency -> BCS1L (SPAC644.07)
no DO ID for isolated_split_hand_split_foot_malformation -> EPS15L1 (SPBC11G11.02c)
no DO ID for kaposiform_hemangioendothelioma -> GNA14 (SPBC24C6.06)
no DO ID for kohlschutter_tonz_syndrome_2 -> SLC13A5 (SPBC3B8.04c)
no DO ID for late_onset_nephronophthisis -> XPNPEP3 (SPAC12B10.05)
no DO ID for leigh_syndrome_with_leukodystrophy -> NDUFV1 (SPBC18E5.10)
no DO ID for leigh_syndrome_with_leukodystrophy -> NDUFV2 (SPAC11E3.12)
no DO ID for leigh_syndrome_with_leukodystrophy -> PDHA1 (SPAC26F1.03)
no DO ID for leigh_syndrome_with_leukodystrophy -> SURF1 (SPBC1215.01)
no DO ID for leigh_syndrome_with_leukodystrophy -> TACO1 (SPBC8D2.12c)
no DO ID for leigh_syndrome_with_leukodystrophy -> SDHA (SPAC1556.02c)
no DO ID for leigh_syndrome_with_leukodystrophy -> MTFMT (SPAC1805.09c)
no DO ID for leigh_syndrome_with_leukodystrophy -> LIPT1 (SPBC17A3.09c)
no DO ID for leigh_syndrome_with_leukodystrophy -> NDUFA9 (SPCC1840.09)
no DO ID for leigh_syndrome_with_leukodystrophy -> NDUFA4 (SPCC417.16)
no DO ID for leigh_syndrome_with_leukodystrophy -> COX15 (SPAC22E12.10c)
no DO ID for leigh_syndrome_with_nephrotic_syndrome -> COQ2 (SPAC56F8.04c)
no DO ID for leukoencephalopathy_hereditary_diffuse_with_spheroids -> AARS2 (SPAC23C11.09)
no DO ID for lipid_storage_myopathy_due_to_flavin_adenine_dinucleotide_synthetase_deficiency -> SLC25A32 (SPBC27B12.09c)
no DO ID for lipid_storage_myopathy_due_to_flavin_adenine_dinucleotide_synthetase_deficiency -> ETFDH (SPAC20G8.04c)
no DO ID for lipid_storage_myopathy_due_to_flavin_adenine_dinucleotide_synthetase_deficiency -> ETFA (SPAC27D7.06)
no DO ID for lipid_storage_myopathy_due_to_flavin_adenine_dinucleotide_synthetase_deficiency -> ETFB (SPAC1805.02c)
no DO ID for low_anorectal_malformation -> MYH14 (SPCC645.05c)
no DO ID for malignant_migrating_partial_seizures_of_infancy -> SLC25A22 (SPCC1682.09c)
no DO ID for malignant_migrating_partial_seizures_of_infancy -> PLCB1 (SPAC22F8.11)
no DO ID for man1b1_cdg -> MAN1B1 (SPAC2E1P5.01c)
no DO ID for maternally_inherited_spastic_paraplegia -> MT-ATP6 (SPMIT.07)
no DO ID for metaphyseal_enchondromatosis_with_d_2_hydroxyglutaric_aciduria -> IDH1 (SPAC6G10.08)
no DO ID for microcephalic_primordial_dwarfism_insulin_resistance_syndrome -> XRCC4 (SPAC6G9.16c)
no DO ID for microcephalic_primordial_dwarfism_insulin_resistance_syndrome -> NSMCE2 (SPAC16A10.06c)
no DO ID for microcephaly_short_stature_intellectual_disability_facial_dysmorphism_syndrome -> QARS (SPBC342.02)
no DO ID for mitochondrial_myopathy_infantile_transient -> TRMU (SPAC23H4.04)
no DO ID for mitochondrial_neurogastrointestinal_encephalomyopathy -> RRM2B (SPBC25D12.04)
no DO ID for mitochondrial_non_syndromic_sensorineural_deafness -> MT-CO1 (SPMIT.01)
no DO ID for mosaic_variegated_aneuploidy_syndrome -> BUB3 (SPAC23H3.08c)
no DO ID for mosaic_variegated_aneuploidy_syndrome -> BUB1 (SPCC1322.12c)
no DO ID for mucopolysaccharidosis_type_6_rapidly_progressing -> ARSB (SPBPB10D8.02c)
no DO ID for mucopolysaccharidosis_type_6_slowly_progressing -> ARSB (SPBPB10D8.02c)
no DO ID for multiple_benign_circumferential_skin_creases_on_limbs -> MAPRE2 (SPAC18G6.15)
no DO ID for multiple_pterygium_syndrome_lethal_type_2 -> NEB (SPAC9G1.06c)
no DO ID for myo5b_related_progressive_familial_intrahepatic_cholestasis -> MYO5B (SPCC1919.10c)
no DO ID for myoclonic_astastic_epilepsy -> CHD2 (SPAC3G6.01)
no DO ID for myopathic_intestinal_pseudoobstruction -> ACTG2 (SPBC32H8.12c)
no DO ID for myopathy_centronuclear_1 -> BIN1 (SPBC21D10.12)
no DO ID for myopathy_lactic_acidosis_and_sideroblastic_anemia_1 -> YARS2 (SPCC576.06c)
no DO ID for nebulin_related_early_onset_distal_myopathy -> NEB (SPAC9G1.06c)
no DO ID for neonatal_adrenoleukodystrophy -> PEX11B (SPBC582.09)
no DO ID for neonatal_glycine_encephalopathy -> GLDC (SPAC13G6.06c)
no DO ID for neonatal_glycine_encephalopathy -> GCSH (SPBP19A11.01)
no DO ID for neonatal_glycine_encephalopathy -> AMT (SPAC31G5.14)
no DO ID for neurofibromatosis_noonan_syndrome -> MAP2K2 (SPAC1D4.13)
no DO ID for neutrophil_specific_granule_deficiency -> SMARCD2 (SPAC23G3.10c)
no DO ID for niemann_pick_disease_type_c_adult_neurologic_onset -> NPC2 (SPAPB8E5.04c)
no DO ID for niemann_pick_disease_type_c_juvenile_neurologic_onset -> NPC2 (SPAPB8E5.04c)
no DO ID for niemann_pick_disease_type_c_late_infantile_neurologic_onset -> NPC2 (SPAPB8E5.04c)
no DO ID for niemann_pick_disease_type_c_severe_early_infantile_neurologic_onset -> NPC2 (SPAPB8E5.04c)
no DO ID for niemann_pick_disease_type_c_severe_perinatal_form -> NPC2 (SPAPB8E5.04c)
no DO ID for nijmegen_breakage_syndrome_like_disorder -> MRE11 (SPAC13C5.07)
no DO ID for non_syndromic_male_infertility_due_to_sperm_motility_disorder -> SLC26A8 (SPBC3H7.02)
no DO ID for optic_atrophy_1 -> DNM1L (SPAC767.01c)
no DO ID for partial_atrioventricular_canal -> GATA6 (SPCC1902.01)
no DO ID for periodic_paralysis_with_later_onset_distal_motor_neuropathy -> MT-ATP8 (SPMIT.09)
no DO ID for periodic_paralysis_with_later_onset_distal_motor_neuropathy -> MT-ATP6 (SPMIT.07)
no DO ID for phakomatosis_pigmentokeratotica -> HRAS (SPAC17H9.09c)
no DO ID for pol_iii_related_leukodystrophies -> POLR3B (SPAC4G9.08c)
no DO ID for pol_iii_related_leukodystrophies -> POLR3A (SPBC651.08c)
no DO ID for pol_iii_related_leukodystrophies -> POLR1C (SPBC1289.07c)
no DO ID for polymerase_proofreading_related_adenomatous_polyposis -> POLE (SPBC25H2.13c)
no DO ID for polymerase_proofreading_related_adenomatous_polyposis -> POLD1 (SPBC336.04)
no DO ID for polymicrogyria_bilateral_perisylvian_x_linked -> PI4KA (SPBC577.06c)
no DO ID for pontocerebellar_hypoplasia_type_1 -> EXOSC8 (SPBC17D1.03c)
no DO ID for pontocerebellar_hypoplasia_type_1 -> RARS2 (SPBC25B2.09c)
no DO ID for porokeratosis_1_multiple_types -> MVK (SPAC13G6.11c)
no DO ID for precursor_t_cell_acute_lymphoblastic_leukemia -> SET (SPBC36B7.08c)
no DO ID for precursor_t_cell_acute_lymphoblastic_leukemia -> DDX3X (SPCC1795.11)
no DO ID for precursor_t_cell_acute_lymphoblastic_leukemia -> CNOT3 (SPAC1B3.05)
no DO ID for prenatal_benign_hypophosphatasia -> ALPL (SPBC14F5.13c)
no DO ID for prenatal_onset_spinal_muscular_atrophy_with_congenital_bone_fractures -> TRIP4 (SPAC1A6.01c)
no DO ID for prenatal_onset_spinal_muscular_atrophy_with_congenital_bone_fractures -> ASCC1 (SPBC15D4.13c)
no DO ID for presynaptic_congenital_myasthenic_syndromes -> SNAP25 (SPBC26H8.02c)
no DO ID for presynaptic_congenital_myasthenic_syndromes -> SLC25A1 (SPAC19G12.05)
no DO ID for primary_hypereosinophilic_syndrome -> FIP1L1 (SPAC22G7.10)
no DO ID for primary_microcephaly_mild_intellectual_disability_young_onset_diabetes_syndrome -> TRMT10A (SPAC6B12.09)
no DO ID for progressive_external_ophthalmoplegia_with_mitochondrial_dna_deletions_autosomal_recessive_2 -> RRM2B (SPBC25D12.04)
no DO ID for psoriasis_14_pustular -> AP1S3 (SPAP27G11.06c)
no DO ID for pulmonary_venoocclusive_disease_1_autosomal_dominant -> EIF2AK4 (SPBC36B7.09)
no DO ID for pustulosis_palmaris_et_plantaris -> AP1S3 (SPAP27G11.06c)
no DO ID for rare_isolated_myopia -> SCO2 (SPBC119.06)
no DO ID for regressive_spondylometaphyseal_dysplasia -> LBR (SPBC16G5.18)
no DO ID for renal_cell_carcinoma_xp11_associated -> PRCC (SPCC4B3.14)
no DO ID for renal_cell_carcinoma_xp11_associated -> ASPSCR1 (SPBC21C3.11)
no DO ID for renal_cell_carcinoma_xp11_associated -> CLTC (SPAC26A3.05)
no DO ID for rh_null_regulator_type -> RHD (SPAC2E1P3.02c)
no DO ID for rh_null_regulator_type -> RHCE (SPAC2E1P3.02c)
no DO ID for rothmund_thomson_syndrome_type_2 -> RECQL4 (SPAC6B12.11)
no DO ID for segmental_outgrowth_lipomatosis_arteriovenous_malformation_epidermal_nevus_syndrome -> PTEN (SPBC609.02)
no DO ID for severe_congenital_nemaline_myopathy -> ACTA1 (SPBC32H8.12c)
no DO ID for severe_early_onset_axonal_neuropathy_due_to_mfn2_deficiency -> MFN2 (SPBC1706.03)
no DO ID for smarca4_deficient_sarcoma_of_thorax -> SMARCA4 (SPCC1620.14c)
no DO ID for spastic_paraplegia_paget_disease_of_bone_syndrome -> VCP (SPAC1565.08)
no DO ID for spinal_muscular_atrophy_with_respiratory_distress_type_2 -> LAS1L (SPBC16C6.12c)
no DO ID for spinocerebellar_ataxia_with_axonal_neuropathy_type_2 -> SETX (SPAC6G9.10c)
no DO ID for spinocerebellar_ataxia_autosomal_recessive_3_2 -> PEX6 (SPAC17A5.01)
no DO ID for spinocerebellar_ataxia_x_linked_5 -> ATP2B3 (SPAPB2B4.04c)
no DO ID for spondyloepimetaphyseal_dysplasia_x_linked_with_mental_deterioration_2 -> AIFM1 (SPAC26F1.14c)
no DO ID for symptomatic_form_of_coffin_lowry_syndrome_in_female_carriers -> RPS6KA3 (SPCC4G3.08)
no DO ID for systemic_lupus_erythematosus_16 -> PRKCD (SPBC12D12.04c)
no DO ID for trichohepatoenteric_syndrome_1 -> SKIV2L (SPCC550.03c)
no DO ID for tubulinopathy_associated_dysgyria -> TUBB3 (SPBC26H8.07c)
no DO ID for tubulinopathy_associated_dysgyria -> TUBB2B (SPBC26H8.07c)
no DO ID for tubulinopathy_associated_dysgyria -> TUBA1A (SPBC16A3.15c)
no DO ID for typical_congenital_nemaline_myopathy -> NEB (SPAC9G1.06c)
no DO ID for typical_congenital_nemaline_myopathy -> CFL2 (SPAC20G4.06c)
no DO ID for typical_congenital_nemaline_myopathy -> ACTA1 (SPBC32H8.12c)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> SLC13A5 (SPBC3B8.04c)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> PPP3CA (SPBP4H10.04)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> NUS1 (SPBC2A9.06c)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> STXBP1 (SPCC584.05)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> SYNJ1 (SPBC2G2.02)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> YWHAG (SPAC17A2.13c)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> UBA5 (SPAC1A6.10)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> AARS (SPAC23C11.09)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> CNKSR2 (SPBC1289.04c)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> DHDDS (SPAC4D7.04c)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> CLTC (SPAC26A3.05)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> AP3B2 (SPAC23H3.06)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> DNM1 (SPAC767.01c)
no DO ID for undetermined_early_onset_epileptic_encephalopathy -> EEF1A2 (SPAC23A1.10)
no DO ID for x_linked_intellectual_disability_limb_spasticity_retinal_dystrophy_diabetes_insipidus_syndrome -> PRPS1 (SPCC1620.06c)
no DO ID for x_linked_non_specific_intellectual_disability -> RPS6KA3 (SPCC4G3.08)
no DO ID for x_linked_non_specific_intellectual_disability -> PAK3 (SPAC1F5.09c)
no DO ID for x_linked_non_specific_intellectual_disability -> ACSL4 (SPBP4H10.11c)
no DO ID for x_linked_non_specific_intellectual_disability -> UPF3B (SPAC13G7.03)
no DO ID for x_linked_non_specific_intellectual_disability -> ALG13 (SPAC56E4.02c)
no DO ID for x_linked_non_specific_intellectual_disability -> CNKSR2 (SPBC1289.04c)
no DO ID for x_linked_non_specific_intellectual_disability -> CLCN4 (SPBC887.02)
no DO ID for x_linked_non_specific_intellectual_disability -> FTSJ1 (SPAC4F10.03c)
no DO ID for x_linked_non_specific_intellectual_disability -> GDI1 (SPAC22H10.12c)
no DO ID for x_linked_non_syndromic_sensorineural_deafness_type_dfn -> PRPS1 (SPCC1620.06c)
no DO ID for zinc_elevated_plasma -> PSTPIP1 (SPBC11C11.02)
no DO ID for fetal_akinesia_deformation_sequence -> TUBB2B (SPBC26H8.07c)
no DO ID for cardiomyopathy_infantile_hypertrophic -> MT-ATP8 (SPMIT.09)
no DO ID for glioma_susceptibility_1 -> H3F3A (SPBC1105.11c)
no DO ID for glioma_susceptibility_1 -> IDH2 (SPAC6G10.08)
no DO ID for glioma_susceptibility_1 -> HIST1H3A (SPBC1105.11c)
no DO ID for limb_girdle_muscular_dystrophy -> DYSF (SPAC1296.04)
no DO ID for alpha_ketoglutarate_dehydrogenase_deficiency -> OGDH (SPBC3H7.03c)
no DO ID for acetyl_coa_carboxylase_deficiency -> ACACA (SPAC56E4.04c)
no DO ID for thrombocytopenia_2 -> MASTL (SPAPB18E9.02c)
no DO ID for essential_pentosuria -> DCXR (SPAC4H3.08)
no DO ID for muscular_dystrophy_dystroglycanopathy_congenital_with_brain_and_eye_anomalies_type_a_1 -> POMT2 (SPAC22A12.07c)
no DO ID for deafness_nonsyndromic_sensorineural_mitochondrial -> MT-CO1 (SPMIT.01)
no DO ID for antley_bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis -> POR (SPBC29A10.01)
no DO ID for chromosome_4p_deletion -> LETM1 (SPAC23C11.17)
no DO ID for congenital_myasthenic_syndrome_associated_with_acetylcholine_receptor_deficiency -> GFPT1 (SPBC12C2.11)
no DO ID for cornelia_de_lange_syndrome_1 -> RAD21 (SPCC338.17c)
no DO ID for giant_congenital_nevus -> HRAS (SPAC17H9.09c)
no DO ID for hereditary_hearing_loss_and_deafness -> PRPS1 (SPCC1620.06c)
no DO ID for hereditary_hearing_loss_and_deafness -> MT-CO1 (SPMIT.01)
no DO ID for mitochondrial_dna_associated_leigh_syndrome_and_narp -> MT-CO3 (SPMIT.04)
no DO ID for mitochondrial_dna_associated_leigh_syndrome_and_narp -> MT-ATP6 (SPMIT.07)
no DO ID for opioid_dependence_1 -> ME2 (SPCC794.12c)
no DO ID for panic_disorder_1 -> COMT (SPBC119.03)
no DO ID for spermatogenic_failure_y_linked_2 -> RPS4Y2 (SPBC21B10.10)
no DO ID for spermatogenic_failure_y_linked_2 -> DDX3Y (SPCC1795.11)
no DO ID for spermatogenic_failure_y_linked_2 -> CDY1 (SPAC4G9.06c)
no DO ID for spermatogenic_failure_y_linked_2 -> CDY2A (SPAC4G9.06c)
no DO ID for spermatogenic_failure_y_linked_2 -> KDM5D (SPAC343.11c)
no DO ID for tracheoesophageal_fistula -> ERCC4 (SPCC970.01)
no DO ID for tracheoesophageal_fistula -> SLX4 (SPAC688.06c)
no DO ID for tracheoesophageal_fistula -> FANCM (SPAC20H4.04)