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About:
Genetic diseases and disorders
An Entity of Type:
Concept
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Property
Value
dbo:
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dbo:
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dbp:
wikiPageUsesTemplate
dbt
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type
skos
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rdfs:
label
Genetic diseases and disorders
(en)
skos:
broader
dbc
:Genetic_genealogy
dbc
:Medical_genetics
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Genetic diseases and disorders
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wikiPageWikiLink
of
dbr
:Camptodactyly-arthropathy-coxa_vara-pericarditis_syndrome
dbr
:Benign_hereditary_chorea
dbr
:Prader–Willi_syndrome
dbr
:Ruijs-Aalfs_syndrome
dbr
:Neuroacanthocytosis
dbr
:MEDNIK_syndrome
dbr
:MPI-CDG
dbr
:Mendelian_susceptibility_to_mycobacterial_disease
dbr
:Metaphyseal_dysostosis-intellectual_disability-conductive_deafness_syndrome
dbr
:Methylenetetrahydrofolate_dehydrogenase_1_deficiency
dbr
:Paroxysmal_nonkinesigenic_dyskinesia
dbr
:Pascual-Castroviejo_syndrome_type_1
dbr
:Smith–Magenis_syndrome
dbr
:Biemond_syndrome
dbr
:Apparent_mineralocorticoid_excess_syndrome
dbr
:Arginine:glycine_amidinotransferase_deficiency
dbr
:Huntington's_disease
dbr
:Hypodysfibrinogenemia
dbr
:List_of_genetic_disorders
dbr
:Curry–Jones_syndrome
dbr
:DAVID_syndrome
dbr
:DDX3X_syndrome
dbr
:DOCK8_deficiency
dbr
:Van_der_Woude_syndrome
dbr
:DeSanto-Shinawi_syndrome
dbr
:De_Barsy_syndrome
dbr
:Deafness-vitiligo-achalasia_syndrome
dbr
:Degenerative_suspensory_ligament_desmitis
dbr
:Dermatoosteolysis,_Kirghizian_type
dbr
:Desmin-related_myofibrillar_myopathy
dbr
:Down_syndrome
dbr
:Dunnigan_familial_partial_lipodystrophy
dbr
:Dwarfism,_low-birth-weight_type_with_unresponsiveness_to_growth_hormone
dbr
:EUROCAT_(medicine)
dbr
:Early-onset_parkinsonism-intellectual_disability_syndrome
dbr
:Inborn_errors_of_steroid_metabolism
dbr
:Infantile_cerebellar_retinal_degeneration
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:Inherited_thrombotic_thrombocytopenic_purpura
dbr
:L1_syndrome
dbr
:Liebenberg_syndrome
dbr
:North_Carolina_macular_dystrophy
dbr
:Reparagen
dbr
:Wiedemann–Steiner_syndrome
dbr
:Common_variable_immunodeficiency
dbr
:Craniometaphyseal_dysplasia
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:Andermann_syndrome
dbr
:Menke-Hennekam_syndrome
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:Genetic_disorder
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:Genetics_of_GnRH_deficiency_conditions
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:Lowry-Wood_syndrome
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:Norrie_disease
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:XMEN_disease
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:RNA-dominant_disease
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:Seaver_Cassidy_syndrome
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:Waardenburg_anophthalmia_syndrome
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:Claire_Wineland
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:Coeliac_disease
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:Enamel-renal_syndrome
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:Glutaminase_deficiency
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:Gordon_syndrome
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:Boucher-Neuhäuser_syndrome
dbr
:Boudhina-Yedes-Khiari_syndrome
dbr
:Brachial_amelia,_cleft_lip,_and_holoprosencephaly
dbr
:Brachydactyly-long_thumb_syndrome
dbr
:Brachydactyly-preaxial_hallux_varus_syndrome
dbr
:Branched-chain_keto_acid_dehydrogenase_kinase_deficiency
dbr
:Branchio-oculo-facial_syndrome
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:NGLY1_deficiency
dbr
:Congenital_adrenal_hyperplasia_due_to_17α-hydroxylase_deficiency
dbr
:Creatine_transporter_defect
dbr
:Cryptorchidism-arachnodactyly-intellectual_disability_syndrome
dbr
:LPS-responsive_beige-like_anchor_protein_deficiency
dbr
:LRBA_deficiency
dbr
:Marsili_syndrome
dbr
:RAS-associated_autoimmune_leukoproliferative_disorder
dbr
:Sotos_syndrome
dbr
:Opitz_G/BBB_syndrome
dbr
:Osteopathia_striata_with_cranial_sclerosis
dbr
:Oto-palato-digital_syndrome
dbr
:Otodental_syndrome
dbr
:Otofaciocervical_syndrome
dbr
:Aromatic_L-amino_acid_decarboxylase_deficiency
dbr
:Chondrodysplasia,_Grebe_type
dbr
:Choroideremia
dbr
:Collins-Pope_syndrome
dbr
:Coloboma_of_macula-brachydactyly_type_B_syndrome
dbr
:Emanuel_syndrome
dbr
:Feigenbaum-Bergeron-Richardson_syndrome
dbr
:Hagemoser–Weinstein–Bresnick_syndrome
dbr
:Hemoglobin_O
dbr
:Joubert_syndrome
dbr
:Kozlowski-Krajewska_syndrome
dbr
:Progeroid_syndromes
dbr
:Small_supernumerary_marker_chromosome
dbr
:Meacham_syndrome
dbr
:Microcephalic_primordial_dwarfism,_Montreal_type
dbr
:Microcephaly_albinism_digital_anomalies_syndrome
dbr
:Microcephaly_lymphoedema_chorioretinal_dysplasia
dbr
:Microcornea,_glaucoma,_and_absent_frontal_sinuses
dbr
:Microspherophakia
dbr
:Muscular_atrophy-ataxia-retinitis_pigmentosa-diabetes_mellitus_syndrome
dbr
:7p22.1_microduplication_syndrome
dbr
:7q11.23_duplication_syndrome
dbr
:Börjeson–Forssman–Lehmann_syndrome
dbr
:Acyl-CoA_oxidase_deficiency
dbr
:Adenosine_deaminase_2_deficiency
dbr
:Cerebral_autosomal_recessive_arteriopa...ical_infarcts_and_leukoencephalopathy
dbr
:Age_of_onset
dbr
:Dauwerse-Peters_syndrome
dbr
:Warfarin_resistance
dbr
:Distal_hereditary_motor_neuropathy_type_V
dbr
:Distal_spinal_muscular_atrophy_type_2
dbr
:Distichiasis,_congenital_heart_defects_and_mixed_peripheral_vascular_anomalies
dbr
:Du_Pan_syndrome
dbr
:GATAD2B-associated_neurodevelopmental_disorder
dbr
:GOSR2-related_progressive_myoclonus_ataxia
dbr
:HFE_H63D_gene_mutation
dbr
:HIDEA_syndrome
dbr
:H_syndrome
dbr
:Heart-hand_syndrome,_Spanish_type
dbr
:Hecht_Scott_syndrome
dbr
:Iris_hypoplasia_with_glaucoma
dbr
:Jones_syndrome
dbr
:Lamb-Shaffer_syndrome
dbr
:Laminopathy
dbr
:Late_onset_congenital_adrenal_hyperplasia
dbr
:SCARF_syndrome
dbr
:Mirror_polydactyly-vertebral_segmentation-limb_defects_syndrome
dbr
:Primrose_syndrome
dbr
:ATR-16_syndrome
dbr
:Al-Raqad_syndrome
dbr
:3-Hydroxyisobutyryl-CoA_deacylase_deficiency
dbr
:3p_deletion_syndrome
dbr
:Al-Gazali-Donnai-Mueller_syndrome
dbr
:Al_Gazali_Sabrinathan_Nair_syndrome
dbr
:Alternating_hemiplegia
dbr
:Alternating_hemiplegia_of_childhood
dbr
:Alwadei_syndrome
dbr
:Amaurosis_congenita,_cone-rod_type,_with_congenital_hypertrichosis
dbr
:Bamforth–Lazarus_syndrome
dbr
:Barakat-Perenthaler_syndrome
dbr
:Brody_myopathy
dbr
:Cardiospondylocarpofacial_syndrome
dbr
:Carey_Fineman_Ziter_syndrome
dbr
:Chronic_enteropathy_associated_with_SLCO2A1_gene
dbr
:Ciliopathy
dbr
:Dilated_cardiomyopathy_with_ataxia_syndrome
dbr
:Familial_dwarfism_and_painful_muscle_spasms
dbr
:Familial_multiple_intestinal_atresia
dbr
:Familial_osteodysplasia,_Anderson_type
dbr
:Fragile_X-associated_primary_ovarian_insufficiency
dbr
:Global_Genes
dbr
:Glycogen_storage_disease_type_IX
dbr
:Goldmann-Favre_syndrome
dbr
:Gollop-Wolfgang_complex
dbr
:Haploinsufficiency_of_A20
dbr
:Hapnes_Boman_Skeie_syndrome
dbr
:Hardcastle_syndrome
dbr
:Hirschsprung's_disease-type_D_brachydactyly_syndrome
dbr
:Isolated_hyperCKemia
dbr
:KCNQ2_developmental_and_epileptic_encephalopathy
dbr
:Kosaki_overgrowth_syndrome
dbr
:List_of_OMIM_disorder_codes
dbr
:Helsmoortel-Van_der_Aa_syndrome
dbr
:Hereditary_diffuse_leukoencephalopathy_with_spheroids
dbr
:Hereditary_haemochromatosis
dbr
:Atelosteogenesis_type_I
dbr
:Costeff_syndrome
dbr
:Cousin_syndrome
dbr
:Cousin–Walbraum–Cegarra_syndrome
dbr
:Huntington's_disease-like_syndrome
dbr
:Hyperglycerolemia
dbr
:Hypertension_and_brachydactyly_syndrome
dbr
:Hypoplasminogenemia
dbr
:Young–Madders_syndrome
dbr
:Snijders_Blok-Campeau_syndrome
dbr
:Smith_Martin_Dodd_syndrome
dbr
:ACDC_(medicine)
dbr
:AFF2
dbr
:ATR-X_syndrome
dbr
:Absence_of_fingerprints-congenital_milia_syndrome
dbr
:Absent_tibia-polydactyly-arachnoid_cyst_syndrome
dbr
:Acrofrontofacionasal_dysostosis
dbr
:Acromesomelic_dysplasia
dbr
:Juvenile_nephronophthisis
dbr
:Keratosis_pilaris
dbr
:Bifid_nose
dbr
:Bilateral_frontoparietal_polymicrogyria
dbr
:Birk-Barel_syndrome
dbr
:Blepharoptosis-myopia-ectopia_lentis_syndrome
dbr
:Blue_cone_monochromacy
dbr
:Cole–Carpenter_syndrome
dbr
:Hereditary_angiopathy_with_nephropathy,_aneurysms,_and_muscle_cramps_syndrome
dbr
:Hereditary_fibrosing_poikiloderma_with...res,_myopathy,_and_pulmonary_fibrosis
dbr
:Holoprosencephaly-ectrodactyly-cleft_lip/palate_syndrome
dbr
:Mitochondrial_complex_II_deficiency
dbr
:Saito-Kuba-Tsuruta_syndrome
dbr
:Tetrasomy_X
dbr
:Thai_symphalangism_syndrome
dbr
:Arthrogryposis_multiplex_with_deafness,_inguinal_hernias,_and_early_death
dbr
:Arts_syndrome
dbr
:Autism_with_port-wine_stain_syndrome
dbr
:Autophagic_vacuolar_myopathy
dbr
:Autosomal_dominant_cerebellar_ataxia,_deafness,_and_narcolepsy
dbr
:Autosomal_dominant_partial_epilepsy_with_auditory_features
dbr
:Autosomal_dominant_porencephaly_type_I
dbr
:Autosomal_recessive_axonal_neuropathy_with_neuromyotonia
dbr
:Autosomal_recessive_bestrophinopathy
dbr
:CDKL5_deficiency_disorder
dbr
:CHAI_disease
dbr
:CHAMP1-associated_intellectual_disability_syndrome
dbr
:CHARGE_syndrome
dbr
:CHDI_Foundation
dbr
:Filippi_syndrome
dbr
:Growth_delay-hydrocephaly-lung_hypoplasia_syndrome
dbr
:Guizar–Vasquez–Sanchez–Manzano_syndrome
dbr
:Thumb_stiffness-brachydactyly-intellectual_disability_syndrome
dbr
:Tibial_hemimelia-polysyndactyly-triphalangeal_thumb_syndrome
dbr
:Warsaw_breakage_syndrome
dbr
:ZC4H2_deficiency
dbr
:Indian_Genetic_Disease_Database
dbr
:Infantile_cortical_hyperostosis
dbr
:Bruck_syndrome
dbr
:Brunner_syndrome
dbr
:Odontoma_dysphagia_syndrome
dbr
:Camera-Marugo-Cohen_syndrome
dbr
:Camptodactyly,_tall_stature,_and_hearing_loss_syndrome
dbr
:Camptodactyly-taurinuria_syndrome
dbr
:Cataract-ataxia-deafness_syndrome
dbr
:ROSAH_syndrome
dbr
:Cerebellar_abiotrophy
dbr
:Cerebral_creatine_deficiency
dbr
:Cerebroretinal_microangiopathy_with_calcifications_and_cysts
dbr
:Sertoli_cell-only_syndrome
dbr
:Wolfram-like_syndrome
dbr
:X-linked_recessive_hypoparathyroidism
dbr
:MDP_syndrome
dbr
:Spinal_muscular_atrophies
dbr
:Shaker_(gene)
dbr
:Variant_of_uncertain_significance
dbr
:Neck-tongue_syndrome
dbr
:Neurocristopathy
dbr
:Swedish_mutation
dbr
:Short-limb_skeletal_dysplasia_with_severe_combined_immunodeficiency
dbr
:FATCO
dbr
:Immunodeficiency_26
dbr
:Ornithine_transcarbamylase_deficiency
dbr
:Oculoauricular_syndrome
dbr
:Oculopharyngodistal_myopathy
dbr
:Ogden_syndrome
dbr
:Olivopontocerebellar_atrophy-deafness_syndrome
dbr
:Schwartz–Jampel_syndrome
dbr
:Primordial_dwarfism
dbr
:Wiedemann–Rautenstrauch_syndrome
dbr
:St._Helena_familial_genu_valgum
dbr
:Sudden_infant_death_with_dysgenesis_of_the_testes_syndrome
dbr
:Tranebjaerg-Svejgaard_syndrome
dbr
:Trigonocephaly-bifid_nose-acral_anomalies_syndrome
dbr
:Myostatin-related_muscle_hypertrophy
dbr
:Nathalie_syndrome
dbr
:Say-Field-Coldwell_syndrome
dbr
:Scalp_defects-postaxial_polydactyly_syndrome
dbr
:Sclerosteosis
dbr
:PASLI_disease
dbr
:Morse–Rawnsley–Sargent_syndrome
dbr
:Multicentric_carpotarsal_osteolysis_syndrome
dbr
:Multiple_congenital_anomalies-hypotonia-seizures_syndrome
dbr
:Multisystem_proteinopathy
dbr
:Pierre_Robin_sequence-faciodigital_anomaly_syndrome
dbr
:Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy
dbr
:Ruzicka_Goerz_Anton_syndrome
dbr
:Sengers_syndrome
dbr
:Sensory_ataxic_neuropathy,_dysarthria,_and_ophthalmoparesis
dbr
:Severe_achondroplasia_with_developmental_delay_and_acanthosis_nigricans
dbr
:Sorsby's_fundus_dystrophy
dbr
:Torsion_dystonia
dbr
:Ulna_hypoplasia-intellectual_disability_syndrome
dbr
:Ulnar_dysplasia
dbr
:Pai_syndrome
dbr
:Qazi–Markouizos_syndrome
dbr
:Retinal_cone_dystrophy_3B
dbr
:Retinal_vasculopathy_with_cerebral_leu...halopathy_and_systemic_manifestations
dbr
:STAT3_GOF
dbr
:STING-associated_vasculopathy_with_onset_in_infancy
dbr
:SYT1-associated_neurodevelopmental_disorder
dbr
:Saal_Greenstein_syndrome
dbr
:X-linked_sideroblastic_anemia_and_spinocerebellar_ataxia
dbr
:XK_aprosencephaly
dbr
:XYYY_syndrome
dbr
:PGM3_deficiency
dbr
:PLAID_syndrome
dbr
:PMM2_deficiency
dbr
:Rhizomelic_dysplasia,_scoliosis,_and_retinitis_pigmentosa
dbr
:Sanjad-Sakati_syndrome
dbr
:Santos-Mateus-Leal_syndrome
dbr
:Teunissen–Cremers_syndrome
dbr
:Small_patella_syndrome
dbr
:Stimmler_syndrome
is
dcterms:
subject
of
dbr
:Camptodactyly-arthropathy-coxa_vara-pericarditis_syndrome
dbr
:Benign_hereditary_chorea
dbr
:Prader–Willi_syndrome
dbr
:Ruijs-Aalfs_syndrome
dbr
:Neuroacanthocytosis
dbr
:MEDNIK_syndrome
dbr
:MPI-CDG
dbr
:Mendelian_susceptibility_to_mycobacterial_disease
dbr
:Metaphyseal_dysostosis-intellectual_disability-conductive_deafness_syndrome
dbr
:Methylenetetrahydrofolate_dehydrogenase_1_deficiency
dbr
:Paroxysmal_nonkinesigenic_dyskinesia
dbr
:Pascual-Castroviejo_syndrome_type_1
dbr
:Smith–Magenis_syndrome
dbr
:Biemond_syndrome
dbr
:Apparent_mineralocorticoid_excess_syndrome
dbr
:Arginine:glycine_amidinotransferase_deficiency
dbr
:Huntington's_disease
dbr
:Hypodysfibrinogenemia
dbr
:List_of_genetic_disorders
dbr
:Curry–Jones_syndrome
dbr
:DAVID_syndrome
dbr
:DDX3X_syndrome
dbr
:DOCK8_deficiency
dbr
:Van_der_Woude_syndrome
dbr
:DeSanto-Shinawi_syndrome
dbr
:De_Barsy_syndrome
dbr
:Deafness-vitiligo-achalasia_syndrome
dbr
:Degenerative_suspensory_ligament_desmitis
dbr
:Dermatoosteolysis,_Kirghizian_type
dbr
:Desmin-related_myofibrillar_myopathy
dbr
:Down_syndrome
dbr
:Dunnigan_familial_partial_lipodystrophy
dbr
:Dwarfism,_low-birth-weight_type_with_unresponsiveness_to_growth_hormone
dbr
:EUROCAT_(medicine)
dbr
:Early-onset_parkinsonism-intellectual_disability_syndrome
dbr
:Inborn_errors_of_steroid_metabolism
dbr
:Infantile_cerebellar_retinal_degeneration
dbr
:Inherited_thrombotic_thrombocytopenic_purpura
dbr
:L1_syndrome
dbr
:Liebenberg_syndrome
dbr
:North_Carolina_macular_dystrophy
dbr
:Reparagen
dbr
:Wiedemann–Steiner_syndrome
dbr
:Common_variable_immunodeficiency
dbr
:Craniometaphyseal_dysplasia
dbr
:Andermann_syndrome
dbr
:Menke-Hennekam_syndrome
dbr
:Genetic_disorder
dbr
:Genetics_of_GnRH_deficiency_conditions
dbr
:Lowry-Wood_syndrome
dbr
:Norrie_disease
dbr
:XMEN_disease
dbr
:RIDDLE_syndrome
dbr
:RNA-dominant_disease
dbr
:Radio-renal_syndrome
dbr
:Seaver_Cassidy_syndrome
dbr
:Waardenburg_anophthalmia_syndrome
dbr
:Claire_Wineland
dbr
:Coeliac_disease
dbr
:Enamel-renal_syndrome
dbr
:Glutaminase_deficiency
dbr
:Gordon_syndrome
dbr
:Boucher-Neuhäuser_syndrome
dbr
:Boudhina-Yedes-Khiari_syndrome
dbr
:Brachial_amelia,_cleft_lip,_and_holoprosencephaly
dbr
:Brachydactyly-long_thumb_syndrome
dbr
:Brachydactyly-preaxial_hallux_varus_syndrome
dbr
:Branched-chain_keto_acid_dehydrogenase_kinase_deficiency
dbr
:Branchio-oculo-facial_syndrome
dbr
:NGLY1_deficiency
dbr
:Congenital_adrenal_hyperplasia_due_to_17α-hydroxylase_deficiency
dbr
:Creatine_transporter_defect
dbr
:Cryptorchidism-arachnodactyly-intellectual_disability_syndrome
dbr
:LPS-responsive_beige-like_anchor_protein_deficiency
dbr
:LRBA_deficiency
dbr
:Marsili_syndrome
dbr
:RAS-associated_autoimmune_leukoproliferative_disorder
dbr
:Sotos_syndrome
dbr
:Opitz_G/BBB_syndrome
dbr
:Osteopathia_striata_with_cranial_sclerosis
dbr
:Oto-palato-digital_syndrome
dbr
:Otodental_syndrome
dbr
:Otofaciocervical_syndrome
dbr
:Aromatic_L-amino_acid_decarboxylase_deficiency
dbr
:Chondrodysplasia,_Grebe_type
dbr
:Choroideremia
dbr
:Collins-Pope_syndrome
dbr
:Coloboma_of_macula-brachydactyly_type_B_syndrome
dbr
:Emanuel_syndrome
dbr
:Feigenbaum-Bergeron-Richardson_syndrome
dbr
:Hagemoser–Weinstein–Bresnick_syndrome
dbr
:Hemoglobin_O
dbr
:Joubert_syndrome
dbr
:Kozlowski-Krajewska_syndrome
dbr
:Progeroid_syndromes
dbr
:Small_supernumerary_marker_chromosome
dbr
:Meacham_syndrome
dbr
:Microcephalic_primordial_dwarfism,_Montreal_type
dbr
:Microcephaly_albinism_digital_anomalies_syndrome
dbr
:Microcephaly_lymphoedema_chorioretinal_dysplasia
dbr
:Microcornea,_glaucoma,_and_absent_frontal_sinuses
dbr
:Microspherophakia
dbr
:Muscular_atrophy-ataxia-retinitis_pigmentosa-diabetes_mellitus_syndrome
dbr
:7p22.1_microduplication_syndrome
dbr
:7q11.23_duplication_syndrome
dbr
:Börjeson–Forssman–Lehmann_syndrome
dbr
:Acyl-CoA_oxidase_deficiency
dbr
:Adenosine_deaminase_2_deficiency
dbr
:Cerebral_autosomal_recessive_arteriopa...ical_infarcts_and_leukoencephalopathy
dbr
:Age_of_onset
dbr
:Dauwerse-Peters_syndrome
dbr
:Warfarin_resistance
dbr
:Distal_hereditary_motor_neuropathy_type_V
dbr
:Distal_spinal_muscular_atrophy_type_2
dbr
:Distichiasis,_congenital_heart_defects_and_mixed_peripheral_vascular_anomalies
dbr
:Du_Pan_syndrome
dbr
:GATAD2B-associated_neurodevelopmental_disorder
dbr
:GOSR2-related_progressive_myoclonus_ataxia
dbr
:HFE_H63D_gene_mutation
dbr
:HIDEA_syndrome
dbr
:H_syndrome
dbr
:Heart-hand_syndrome,_Spanish_type
dbr
:Hecht_Scott_syndrome
dbr
:Iris_hypoplasia_with_glaucoma
dbr
:Jones_syndrome
dbr
:Lamb-Shaffer_syndrome
dbr
:Laminopathy
dbr
:Late_onset_congenital_adrenal_hyperplasia
dbr
:SCARF_syndrome
dbr
:Mirror_polydactyly-vertebral_segmentation-limb_defects_syndrome
dbr
:Primrose_syndrome
dbr
:ATR-16_syndrome
dbr
:Al-Raqad_syndrome
dbr
:3-Hydroxyisobutyryl-CoA_deacylase_deficiency
dbr
:3p_deletion_syndrome
dbr
:Al-Gazali-Donnai-Mueller_syndrome
dbr
:Al_Gazali_Sabrinathan_Nair_syndrome
dbr
:Alternating_hemiplegia
dbr
:Alternating_hemiplegia_of_childhood
dbr
:Alwadei_syndrome
dbr
:Amaurosis_congenita,_cone-rod_type,_with_congenital_hypertrichosis
dbr
:Bamforth–Lazarus_syndrome
dbr
:Barakat-Perenthaler_syndrome
dbr
:Brody_myopathy
dbr
:Cardiospondylocarpofacial_syndrome
dbr
:Carey_Fineman_Ziter_syndrome
dbr
:Chronic_enteropathy_associated_with_SLCO2A1_gene
dbr
:Ciliopathy
dbr
:Dilated_cardiomyopathy_with_ataxia_syndrome
dbr
:Familial_dwarfism_and_painful_muscle_spasms
dbr
:Familial_multiple_intestinal_atresia
dbr
:Familial_osteodysplasia,_Anderson_type
dbr
:Fragile_X-associated_primary_ovarian_insufficiency
dbr
:Global_Genes
dbr
:Glycogen_storage_disease_type_IX
dbr
:Goldmann-Favre_syndrome
dbr
:Gollop-Wolfgang_complex
dbr
:Haploinsufficiency_of_A20
dbr
:Hapnes_Boman_Skeie_syndrome
dbr
:Hardcastle_syndrome
dbr
:Hirschsprung's_disease-type_D_brachydactyly_syndrome
dbr
:Isolated_hyperCKemia
dbr
:KCNQ2_developmental_and_epileptic_encephalopathy
dbr
:Kosaki_overgrowth_syndrome
dbr
:List_of_OMIM_disorder_codes
dbr
:Helsmoortel-Van_der_Aa_syndrome
dbr
:Hereditary_diffuse_leukoencephalopathy_with_spheroids
dbr
:Hereditary_haemochromatosis
dbr
:Atelosteogenesis_type_I
dbr
:Costeff_syndrome
dbr
:Cousin_syndrome
dbr
:Cousin–Walbraum–Cegarra_syndrome
dbr
:Huntington's_disease-like_syndrome
dbr
:Hyperglycerolemia
dbr
:Hypertension_and_brachydactyly_syndrome
dbr
:Hypoplasminogenemia
dbr
:Young–Madders_syndrome
dbr
:Snijders_Blok-Campeau_syndrome
dbr
:Smith_Martin_Dodd_syndrome
dbr
:ACDC_(medicine)
dbr
:AFF2
dbr
:ATR-X_syndrome
dbr
:Absence_of_fingerprints-congenital_milia_syndrome
dbr
:Absent_tibia-polydactyly-arachnoid_cyst_syndrome
dbr
:Acrofrontofacionasal_dysostosis
dbr
:Acromesomelic_dysplasia
dbr
:Juvenile_nephronophthisis
dbr
:Keratosis_pilaris
dbr
:Bifid_nose
dbr
:Bilateral_frontoparietal_polymicrogyria
dbr
:Birk-Barel_syndrome
dbr
:Blepharoptosis-myopia-ectopia_lentis_syndrome
dbr
:Blue_cone_monochromacy
dbr
:Cole–Carpenter_syndrome
dbr
:Hereditary_angiopathy_with_nephropathy,_aneurysms,_and_muscle_cramps_syndrome
dbr
:Hereditary_fibrosing_poikiloderma_with...res,_myopathy,_and_pulmonary_fibrosis
dbr
:Holoprosencephaly-ectrodactyly-cleft_lip/palate_syndrome
dbr
:Mitochondrial_complex_II_deficiency
dbr
:Saito-Kuba-Tsuruta_syndrome
dbr
:Tetrasomy_X
dbr
:Thai_symphalangism_syndrome
dbr
:Arthrogryposis_multiplex_with_deafness,_inguinal_hernias,_and_early_death
dbr
:Arts_syndrome
dbr
:Autism_with_port-wine_stain_syndrome
dbr
:Autophagic_vacuolar_myopathy
dbr
:Autosomal_dominant_cerebellar_ataxia,_deafness,_and_narcolepsy
dbr
:Autosomal_dominant_partial_epilepsy_with_auditory_features
dbr
:Autosomal_dominant_porencephaly_type_I
dbr
:Autosomal_recessive_axonal_neuropathy_with_neuromyotonia
dbr
:Autosomal_recessive_bestrophinopathy
dbr
:CDKL5_deficiency_disorder
dbr
:CHAI_disease
dbr
:CHAMP1-associated_intellectual_disability_syndrome
dbr
:CHARGE_syndrome
dbr
:CHDI_Foundation
dbr
:Filippi_syndrome
dbr
:Growth_delay-hydrocephaly-lung_hypoplasia_syndrome
dbr
:Guizar–Vasquez–Sanchez–Manzano_syndrome
dbr
:Thumb_stiffness-brachydactyly-intellectual_disability_syndrome
dbr
:Tibial_hemimelia-polysyndactyly-triphalangeal_thumb_syndrome
dbr
:Warsaw_breakage_syndrome
dbr
:ZC4H2_deficiency
dbr
:Indian_Genetic_Disease_Database
dbr
:Infantile_cortical_hyperostosis
dbr
:Bruck_syndrome
dbr
:Brunner_syndrome
dbr
:Odontoma_dysphagia_syndrome
dbr
:Camera-Marugo-Cohen_syndrome
dbr
:Camptodactyly,_tall_stature,_and_hearing_loss_syndrome
dbr
:Camptodactyly-taurinuria_syndrome
dbr
:Cataract-ataxia-deafness_syndrome
dbr
:ROSAH_syndrome
dbr
:Cerebellar_abiotrophy
dbr
:Cerebral_creatine_deficiency
dbr
:Cerebroretinal_microangiopathy_with_calcifications_and_cysts
dbr
:Sertoli_cell-only_syndrome
dbr
:Wolfram-like_syndrome
dbr
:X-linked_recessive_hypoparathyroidism
dbr
:MDP_syndrome
dbr
:Spinal_muscular_atrophies
dbr
:Shaker_(gene)
dbr
:Variant_of_uncertain_significance
dbr
:Neck-tongue_syndrome
dbr
:Neurocristopathy
dbr
:Swedish_mutation
dbr
:Short-limb_skeletal_dysplasia_with_severe_combined_immunodeficiency
dbr
:FATCO
dbr
:Immunodeficiency_26
dbr
:Ornithine_transcarbamylase_deficiency
dbr
:Oculoauricular_syndrome
dbr
:Oculopharyngodistal_myopathy
dbr
:Ogden_syndrome
dbr
:Olivopontocerebellar_atrophy-deafness_syndrome
dbr
:Schwartz–Jampel_syndrome
dbr
:Primordial_dwarfism
dbr
:Wiedemann–Rautenstrauch_syndrome
dbr
:St._Helena_familial_genu_valgum
dbr
:Sudden_infant_death_with_dysgenesis_of_the_testes_syndrome
dbr
:Tranebjaerg-Svejgaard_syndrome
dbr
:Trigonocephaly-bifid_nose-acral_anomalies_syndrome
dbr
:Myostatin-related_muscle_hypertrophy
dbr
:Nathalie_syndrome
dbr
:Say-Field-Coldwell_syndrome
dbr
:Scalp_defects-postaxial_polydactyly_syndrome
dbr
:Sclerosteosis
dbr
:PASLI_disease
dbr
:Morse–Rawnsley–Sargent_syndrome
dbr
:Multicentric_carpotarsal_osteolysis_syndrome
dbr
:Multiple_congenital_anomalies-hypotonia-seizures_syndrome
dbr
:Multisystem_proteinopathy
dbr
:Pierre_Robin_sequence-faciodigital_anomaly_syndrome
dbr
:Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy
dbr
:Ruzicka_Goerz_Anton_syndrome
dbr
:Sengers_syndrome
dbr
:Sensory_ataxic_neuropathy,_dysarthria,_and_ophthalmoparesis
dbr
:Severe_achondroplasia_with_developmental_delay_and_acanthosis_nigricans
dbr
:Sorsby's_fundus_dystrophy
dbr
:Torsion_dystonia
dbr
:Ulna_hypoplasia-intellectual_disability_syndrome
dbr
:Ulnar_dysplasia
dbr
:Pai_syndrome
dbr
:Qazi–Markouizos_syndrome
dbr
:Retinal_cone_dystrophy_3B
dbr
:Retinal_vasculopathy_with_cerebral_leu...halopathy_and_systemic_manifestations
dbr
:STAT3_GOF
dbr
:STING-associated_vasculopathy_with_onset_in_infancy
dbr
:SYT1-associated_neurodevelopmental_disorder
dbr
:Saal_Greenstein_syndrome
dbr
:X-linked_sideroblastic_anemia_and_spinocerebellar_ataxia
dbr
:XK_aprosencephaly
dbr
:XYYY_syndrome
dbr
:PGM3_deficiency
dbr
:PLAID_syndrome
dbr
:PMM2_deficiency
dbr
:Rhizomelic_dysplasia,_scoliosis,_and_retinitis_pigmentosa
dbr
:Sanjad-Sakati_syndrome
dbr
:Santos-Mateus-Leal_syndrome
dbr
:Teunissen–Cremers_syndrome
dbr
:Small_patella_syndrome
dbr
:Stimmler_syndrome
is
skos:
broader
of
dbc
:Genetic_disorders_by_mechanism
dbc
:People_with_genetic_disorders
dbc
:Genetic_animal_diseases
dbc
:Genetic_disorder_stubs
dbc
:Genetic_disorders_by_inheritance
dbc
:Genetic_anomalies
dbc
:Genetic_disorders_with_known_gene_but_no_known_gene_function
dbc
:Single-nucleotide_polymorphism_associated_disease
dbc
:Genetic_disorders_with_no_OMIM
dbc
:Genetic_syndromes
dbc
:Genetic_disorders_with_OMIM_but_no_gene
dbc
:Genetic_disorders_by_system
dbc
:Progeroid_syndromes
dbc
:Inherited_disorders_of_trafficking
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