About: Congenital disorders

Property	Value
dbo:wikiPageID	966400 (xsd:integer)
dbo:wikiPageRevisionID	954469150 (xsd:integer)
dbp:wikiPageUsesTemplate	dbt:Commons_category dbt:CatAutoTOC dbt:Cat_main dbt:ICD_category
rdf:type	skos:Concept
rdfs:label	Congenital disorders (en)
skos:broader	dbc:Animal_diseases dbc:Pediatrics dbc:Genetics dbc:Disability_by_type
skos:prefLabel	Congenital disorders (en)
prov:wasDerivedFrom	wikipedia-en:Category:Congenital_disorders?oldid=954469150&ns=14
is dbo:wikiPageWikiLink of	dbr:Prader–Willi_syndrome dbr:Proboscis_(anomaly) dbr:Progressive_familial_intrahepatic_cholestasis dbr:Proteus_syndrome dbr:Rubinstein–Taybi_syndrome dbr:List_of_congenital_disorders dbr:Neuronal_ceroid_lipofuscinosis dbr:MORM_syndrome dbr:MURCS_association dbr:Meningohydroencephalocoele dbr:Meromelia dbr:Monstrous_birth dbr:Primary_congenital_lymphedema dbr:Progressive_cardiac_conduction_defect dbr:Saethre–Chotzen_syndrome dbr:Bartter_syndrome dbr:Allogeneic_processed_thymus_tissue dbr:Animal_chimerism dbr:Anorectal_anomalies dbr:Arachnoid_cyst dbr:Archibald's_sign dbr:Holt–Oram_syndrome dbr:Bhaskar–Jagannathan_syndrome dbr:Char_syndrome dbr:Cyclopia dbr:Cystic_hygroma dbr:D-glycerate_dehydrogenase_deficiency dbr:Ulnar_dimelia dbr:Umbilical_cord_ulceration_and_intestinal_atresia dbr:Van_der_Woude_syndrome dbr:Dopamine-responsive_dystonia dbr:Kvikk_case dbr:Ponseti_method dbr:Pelvic_digit dbr:Potocki–Lupski_syndrome dbr:Pterin-4_alpha-carbinolamine_dehydratase_deficiency dbr:North_Carolina_macular_dystrophy dbr:Congenital_iodine_deficiency_syndrome dbr:Congenital_nephrotic_syndrome dbr:Crandall_syndrome dbr:Amyoplasia dbr:Palatal_obturator dbr:Thumb_hypoplasia dbr:Simpson–Golabi–Behmel_syndrome dbr:Vestigial_twin dbr:Vici_syndrome dbr:RIDDLE_syndrome dbr:Waardenburg_Syndrome_Type_1 dbr:Ehlers–Danlos_syndromes dbr:Endocardial_fibroelastosis dbr:Genitoplasty dbr:Bowen–Conradi_syndrome dbr:Nager_acrofacial_dysostosis dbr:Congenital_afibrinogenemia dbr:Congenital_athymia dbr:Congenital_fiber_type_disproportion dbr:Congenital_hypofibrinogenemia dbr:Congenital_malaria dbr:Congenital_rubella_syndrome dbr:Constriction_ring_syndrome dbr:Osteochondroprogenitor_cell dbr:Ostravik-Lindemann-Solberg_syndrome dbr:Benjamin_syndrome dbr:Cleft_palate_incidence_by_population dbr:Clitoridectomy dbr:Denis_Browne_bar dbr:Zadik–Barak–Levin_syndrome dbr:Femur_fibula_ulna_syndrome dbr:Hajdu–Cheney_syndrome dbr:Hemifacial_microsomia dbr:Keutel_syndrome dbr:Patterson_syndrome dbr:Pfeiffer_syndrome dbr:Mature_teratoma dbr:Maturity-onset_diabetes_of_the_young dbr:McCune–Albright_syndrome dbr:Multiple_abnormalities dbr:Potocki–Shaffer_syndrome dbr:Muscle–eye–brain_disease dbr:Ayazi_syndrome dbr:CANDLE_syndrome dbr:Agenesis dbr:Trichothiodystrophy dbr:Hearing_loss_with_craniofacial_syndromes dbr:Laryngeal_cleft dbr:Late_congenital_syphilitic_oculopathy dbr:Rudiger_syndrome dbr:Urofacial_syndrome dbr:Shprintzen–Goldberg_syndrome dbr:Achondrogenesis dbr:Achondroplasia_in_children dbr:Duane_syndrome dbr:Dyskeratosis_congenita dbr:Ectopic_pancreas dbr:Fetal_trimethadione_syndrome dbr:Fibrodysplasia_ossificans_progressiva dbr:Bangstad_syndrome dbr:Barakat_syndrome dbr:Niemann–Pick_disease dbr:Caudal_duplication dbr:Caudal_regression_syndrome dbr:Diprosopus dbr:Dipygus dbr:Familial_male-limited_precocious_puberty dbr:Goldberg–Shprintzen_syndrome dbr:Goldenhar_syndrome dbr:Isodisomy dbr:Juberg-Hayward_syndrome dbr:Katz_syndrome dbr:Kaufman_oculocerebrofacial_syndrome dbr:Kniest_dysplasia dbr:Persistent_cloaca dbr:Miller–Dieker_syndrome dbr:Smith–Fineman–Myers_syndrome dbr:1q21.1_copy_number_variations dbr:1q21.1_deletion_syndrome dbr:Halal_syndrome dbr:Halperin-Birk_syndrome dbr:Hemifacial_hypertrophy dbr:Atransferrinemia dbr:Isolated_congenital_asplenia dbr:Tay–Sachs_disease dbr:Craniofacial_cleft dbr:Craniopagus_parasiticus dbr:Teratoma dbr:Hydrolethalus_syndrome dbr:Marden–Walker_syndrome dbr:Marfanoid dbr:Sepiapterin_reductase_deficiency dbr:Snyder–Robinson_syndrome dbr:Aagenaes_syndrome dbr:Aarskog–Scott_syndrome dbr:Achondrogenesis_type_1B dbr:Achondrogenesis_type_2 dbr:Acrodysostosis dbr:Alcohol_and_pregnancy dbr:Langer_mesomelic_dysplasia dbr:Birth_defect dbr:Heterotopia_(medicine) dbr:TORCH_syndrome dbr:Transposition_(birth_defect) dbr:Worth_syndrome dbr:Triple-A_syndrome dbr:Arterial_calcification_due_to_CD73_deficiency dbr:Asplenia_with_cardiovascular_anomalies dbr:Autosomal_dominant_GTP_cyclohydrolase_I_deficiency dbr:Autosomal_recessive_GTP_cyclohydrolase_I_deficiency dbr:Boomerang_dysplasia dbr:Bosch-Boonstra-Schaaf_optic_atrophy_syndrome dbr:Burnside–Butler_syndrome dbr:CAMFAK_syndrome dbr:Pilotto_syndrome dbr:Spondyloepimetaphyseal_dysplasia dbr:Fetus_in_fetu dbr:Fibro-adipose_vascular_anomaly dbr:Fibrochondrogenesis dbr:Filippi_syndrome dbr:Guizar–Vasquez–Sanchez–Manzano_syndrome dbr:Ho–Kaufman–Mcalister_syndrome dbr:Tyrosine_hydroxylase_deficiency dbr:Michels_syndrome dbr:Brugada_syndrome dbr:Neu–Laxova_syndrome dbr:Camptodactyly dbr:Cat_eye_syndrome dbr:Radioulnar_synostosis dbr:Senior–Løken_syndrome dbr:XX_male_syndrome dbr:MDP_syndrome dbr:Majewski's_polydactyly_syndrome dbr:Minor_physical_anomalies dbr:Sacrococcygeal_teratoma dbr:Marinesco–Sjögren_syndrome dbr:SHORT_syndrome dbr:Seckel_syndrome dbr:Sequence_(medicine) dbr:Situs_ambiguus dbr:Situs_inversus dbr:Neonatal_teeth dbr:Neurocristopathy dbr:Neurocutaneous_melanosis dbr:VACTERL_association dbr:Wilson–Turner_syndrome dbr:Walker–Warburg_syndrome dbr:Toxocara_malayasiensis dbr:Ethmocephaly dbr:Facial_femoral_syndrome dbr:Faciocardiorenal_syndrome dbr:Factor_I_deficiency dbr:Immunodeficiency_26 dbr:Oculoauricular_syndrome dbr:Sirenomelia dbr:Triploid_syndrome dbr:Weaver_syndrome dbr:Rosselli–Gulienetti_syndrome dbr:Ulas_family dbr:Transient_myeloproliferative_disease dbr:First_arch_syndrome dbr:Fleischer's_syndrome dbr:Malformative_syndrome dbr:Malouf_syndrome dbr:Malpuech_facial_clefting_syndrome dbr:Opsismodysplasia dbr:Myelokathexis dbr:Nakajo_syndrome dbr:Nasodigitoacoustic_syndrome dbr:Triphalangeal_thumb dbr:Muenke_syndrome dbr:Mulibrey_nanism dbr:Zamzam–Sheriff–Phillips_syndrome dbr:Polymelia dbr:Porencephaly dbr:Vaginal_septum dbr:Young–Simpson_syndrome dbr:Spondyloperipheral_dysplasia dbr:Status_marmoratus dbr:Weissenbacher–Zweymüller_syndrome dbr:Norman–Roberts_syndrome dbr:Sacral_dimple dbr:Renal–hepatic–pancreatic_dysplasia dbr:Renal_dysplasia-limb_defects_syndrome dbr:Sacral_agenesis dbr:Orofaciodigital_syndrome_1 dbr:Papillary_fibroelastoma dbr:Parasitic_twin dbr:Parastremmatic_dwarfism dbr:Riboflavin-responsive_exercise_intolerance dbr:Tetra-amelia_syndrome dbr:Velopharyngeal_inadequacy dbr:Ring_chromosome_14_syndrome dbr:Ring_chromosome_15 dbr:Strophosomia dbr:Structural_variation dbr:Spondyloepimetaphyseal_dysplasia,_Strudwick_type
is dct:subject of	dbr:Prader–Willi_syndrome dbr:Proboscis_(anomaly) dbr:Progressive_familial_intrahepatic_cholestasis dbr:Proteus_syndrome dbr:Rubinstein–Taybi_syndrome dbr:List_of_congenital_disorders dbr:Neuronal_ceroid_lipofuscinosis dbr:MORM_syndrome dbr:MURCS_association dbr:Meningohydroencephalocoele dbr:Meromelia dbr:Monstrous_birth dbr:Primary_congenital_lymphedema dbr:Progressive_cardiac_conduction_defect dbr:Saethre–Chotzen_syndrome dbr:Bartter_syndrome dbr:Allogeneic_processed_thymus_tissue dbr:Animal_chimerism dbr:Anorectal_anomalies dbr:Arachnoid_cyst dbr:Archibald's_sign dbr:Holt–Oram_syndrome dbr:Bhaskar–Jagannathan_syndrome dbr:Char_syndrome dbr:Cyclopia dbr:Cystic_hygroma dbr:D-glycerate_dehydrogenase_deficiency dbr:Ulnar_dimelia dbr:Umbilical_cord_ulceration_and_intestinal_atresia dbr:Van_der_Woude_syndrome dbr:Dopamine-responsive_dystonia dbr:Kvikk_case dbr:Ponseti_method dbr:Pelvic_digit dbr:Potocki–Lupski_syndrome dbr:Pterin-4_alpha-carbinolamine_dehydratase_deficiency dbr:North_Carolina_macular_dystrophy dbr:Congenital_iodine_deficiency_syndrome dbr:Congenital_nephrotic_syndrome dbr:Crandall_syndrome dbr:Amyoplasia dbr:Palatal_obturator dbr:Thumb_hypoplasia dbr:Simpson–Golabi–Behmel_syndrome dbr:Vestigial_twin dbr:Vici_syndrome dbr:RIDDLE_syndrome dbr:Waardenburg_Syndrome_Type_1 dbr:Ehlers–Danlos_syndromes dbr:Endocardial_fibroelastosis dbr:Genitoplasty dbr:Bowen–Conradi_syndrome dbr:Nager_acrofacial_dysostosis dbr:Congenital_afibrinogenemia dbr:Congenital_athymia dbr:Congenital_fiber_type_disproportion dbr:Congenital_hypofibrinogenemia dbr:Congenital_malaria dbr:Congenital_rubella_syndrome dbr:Constriction_ring_syndrome dbr:Osteochondroprogenitor_cell dbr:Ostravik-Lindemann-Solberg_syndrome dbr:Benjamin_syndrome dbr:Cleft_palate_incidence_by_population dbr:Clitoridectomy dbr:Denis_Browne_bar dbr:Zadik–Barak–Levin_syndrome dbr:Femur_fibula_ulna_syndrome dbr:Hajdu–Cheney_syndrome dbr:Hemifacial_microsomia dbr:Keutel_syndrome dbr:Patterson_syndrome dbr:Pfeiffer_syndrome dbr:Mature_teratoma dbr:Maturity-onset_diabetes_of_the_young dbr:McCune–Albright_syndrome dbr:Multiple_abnormalities dbr:Potocki–Shaffer_syndrome dbr:Muscle–eye–brain_disease dbr:Ayazi_syndrome dbr:CANDLE_syndrome dbr:Agenesis dbr:Trichothiodystrophy dbr:Hearing_loss_with_craniofacial_syndromes dbr:Laryngeal_cleft dbr:Late_congenital_syphilitic_oculopathy dbr:Rudiger_syndrome dbr:Urofacial_syndrome dbr:Shprintzen–Goldberg_syndrome dbr:Achondrogenesis dbr:Achondroplasia_in_children dbr:Duane_syndrome dbr:Dyskeratosis_congenita dbr:Ectopic_pancreas dbr:Fetal_trimethadione_syndrome dbr:Fibrodysplasia_ossificans_progressiva dbr:Bangstad_syndrome dbr:Barakat_syndrome dbr:Niemann–Pick_disease dbr:Caudal_duplication dbr:Caudal_regression_syndrome dbr:Diprosopus dbr:Dipygus dbr:Familial_male-limited_precocious_puberty dbr:Goldberg–Shprintzen_syndrome dbr:Goldenhar_syndrome dbr:Isodisomy dbr:Juberg-Hayward_syndrome dbr:Katz_syndrome dbr:Kaufman_oculocerebrofacial_syndrome dbr:Kniest_dysplasia dbr:Persistent_cloaca dbr:Miller–Dieker_syndrome dbr:Smith–Fineman–Myers_syndrome dbr:1q21.1_copy_number_variations dbr:1q21.1_deletion_syndrome dbr:Halal_syndrome dbr:Halperin-Birk_syndrome dbr:Hemifacial_hypertrophy dbr:Atransferrinemia dbr:Isolated_congenital_asplenia dbr:Tay–Sachs_disease dbr:Craniofacial_cleft dbr:Craniopagus_parasiticus dbr:Teratoma dbr:Hydrolethalus_syndrome dbr:Marden–Walker_syndrome dbr:Marfanoid dbr:Sepiapterin_reductase_deficiency dbr:Snyder–Robinson_syndrome dbr:Aagenaes_syndrome dbr:Aarskog–Scott_syndrome dbr:Achondrogenesis_type_1B dbr:Achondrogenesis_type_2 dbr:Acrodysostosis dbr:Alcohol_and_pregnancy dbr:Langer_mesomelic_dysplasia dbr:Birth_defect dbr:Heterotopia_(medicine) dbr:TORCH_syndrome dbr:Transposition_(birth_defect) dbr:Worth_syndrome dbr:Triple-A_syndrome dbr:Arterial_calcification_due_to_CD73_deficiency dbr:Asplenia_with_cardiovascular_anomalies dbr:Autosomal_dominant_GTP_cyclohydrolase_I_deficiency dbr:Autosomal_recessive_GTP_cyclohydrolase_I_deficiency dbr:Boomerang_dysplasia dbr:Bosch-Boonstra-Schaaf_optic_atrophy_syndrome dbr:Burnside–Butler_syndrome dbr:CAMFAK_syndrome dbr:Pilotto_syndrome dbr:Spondyloepimetaphyseal_dysplasia dbr:Fetus_in_fetu dbr:Fibro-adipose_vascular_anomaly dbr:Fibrochondrogenesis dbr:Filippi_syndrome dbr:Guizar–Vasquez–Sanchez–Manzano_syndrome dbr:Ho–Kaufman–Mcalister_syndrome dbr:Tyrosine_hydroxylase_deficiency dbr:Michels_syndrome dbr:Brugada_syndrome dbr:Neu–Laxova_syndrome dbr:Camptodactyly dbr:Cat_eye_syndrome dbr:Radioulnar_synostosis dbr:Senior–Løken_syndrome dbr:XX_male_syndrome dbr:MDP_syndrome dbr:Majewski's_polydactyly_syndrome dbr:Minor_physical_anomalies dbr:Sacrococcygeal_teratoma dbr:Marinesco–Sjögren_syndrome dbr:SHORT_syndrome dbr:Seckel_syndrome dbr:Sequence_(medicine) dbr:Situs_ambiguus dbr:Situs_inversus dbr:Neonatal_teeth dbr:Neurocristopathy dbr:Neurocutaneous_melanosis dbr:VACTERL_association dbr:Wilson–Turner_syndrome dbr:Walker–Warburg_syndrome dbr:Toxocara_malayasiensis dbr:Ethmocephaly dbr:Facial_femoral_syndrome dbr:Faciocardiorenal_syndrome dbr:Factor_I_deficiency dbr:Immunodeficiency_26 dbr:Oculoauricular_syndrome dbr:Sirenomelia dbr:Triploid_syndrome dbr:Weaver_syndrome dbr:Rosselli–Gulienetti_syndrome dbr:Ulas_family dbr:Transient_myeloproliferative_disease dbr:First_arch_syndrome dbr:Fleischer's_syndrome dbr:Malformative_syndrome dbr:Malouf_syndrome dbr:Malpuech_facial_clefting_syndrome dbr:Opsismodysplasia dbr:Myelokathexis dbr:Nakajo_syndrome dbr:Nasodigitoacoustic_syndrome dbr:Triphalangeal_thumb dbr:Muenke_syndrome dbr:Mulibrey_nanism dbr:Zamzam–Sheriff–Phillips_syndrome dbr:Polymelia dbr:Porencephaly dbr:Vaginal_septum dbr:Young–Simpson_syndrome dbr:Spondyloperipheral_dysplasia dbr:Status_marmoratus dbr:Weissenbacher–Zweymüller_syndrome dbr:Norman–Roberts_syndrome dbr:Sacral_dimple dbr:Renal–hepatic–pancreatic_dysplasia dbr:Renal_dysplasia-limb_defects_syndrome dbr:Sacral_agenesis dbr:Orofaciodigital_syndrome_1 dbr:Papillary_fibroelastoma dbr:Parasitic_twin dbr:Parastremmatic_dwarfism dbr:Riboflavin-responsive_exercise_intolerance dbr:Tetra-amelia_syndrome dbr:Velopharyngeal_inadequacy dbr:Ring_chromosome_14_syndrome dbr:Ring_chromosome_15 dbr:Strophosomia dbr:Structural_variation dbr:Spondyloepimetaphyseal_dysplasia,_Strudwick_type
is skos:broader of	dbc:Fictional_characters_with_physical_and_congenital_disorders dbc:Congenital_disorders_of_genital_organs dbc:Congenital_disorders_of_circulatory_system dbc:Ehlers–Danlos_syndrome dbc:Congenital_malformation_due_to_exogenous_toxicity dbc:Inborn_errors_of_metabolism dbc:Cystic_fibrosis dbc:Cutaneous_congenital_anomalies dbc:Congenital_disorders_of_musculoskeletal_system dbc:Congenital_disorders_of_breasts dbc:Congenital_disorders_of_digestive_system dbc:Congenital_disorders_of_endocrine_system dbc:Congenital_disorders_of_nervous_system dbc:Teratogens dbc:Albinism dbc:Congenital_disorders_of_urinary_system dbc:Congenital_disorders_of_respiratory_system dbc:Congenital_disorders_of_eye,_ear,_face_and_neck dbc:Fibrodysplasia_ossificans_progressiva