WikicatGeneticDisorders

An Entity of Type: Thing, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Property	Value
rdfs:subClassOf	yago:GeneticDisease114151139
owl:equivalentClass	yago-res:wikicat_Genetic_disorders
is rdf:type of	dbr:Camptodactyly-arthropathy-coxa_vara-pericarditis_syndrome dbr:Camurati–Engelmann_disease dbr:Carney_complex dbr:Carnitine_palmitoyltransferase_II_deficiency dbr:Caroli_disease dbr:Cartilage–hair_hypoplasia dbr:Catecholaminergic_polymorphic_ventricular_tachycardia dbr:Amelogenesis_imperfecta dbr:Aminolevulinic_acid_dehydratase_deficiency_porphyria dbr:48,_XXXX dbr:49,_XXXXX dbr:5-alpha-reductase_deficiency dbr:Beckwith–Wiedemann_syndrome dbr:Prader–Willi_syndrome dbr:Primary_ciliary_dyskinesia dbr:Proteus_syndrome dbr:Pseudohypoparathyroidism dbr:Pseudoxanthoma_elasticum dbr:Rubinstein–Taybi_syndrome dbr:Sandhoff_disease dbr:Sanfilippo_syndrome dbr:Schindler_disease dbr:Epidermolysis_bullosa dbr:Epidermolysis_bullosa_dystrophica dbr:Epilepsy-intellectual_disability_in_females dbr:Epileptic_spasms dbr:MELAS_syndrome dbr:MOMO_syndrome dbr:Mitochondrial_disease dbr:Mosaic_(genetics) dbr:Moyamoya_disease dbr:Muckle–Wells_syndrome dbr:Multiple_endocrine_neoplasia dbr:Myhre_syndrome dbr:Neuroacanthocytosis dbr:Neuronal_ceroid_lipofuscinosis dbr:Nijmegen_breakage_syndrome dbr:Lytico-bodig_disease dbr:Léri–Weill_dyschondrosteosis dbr:MERRF_syndrome dbr:Meleda_disease dbr:Melnick–Needles_syndrome dbr:Metachromatic_leukodystrophy dbr:Morgagni_Stewart_Morel_syndrome dbr:Nephronophthisis dbr:Omenn_syndrome dbr:Paroxysmal_nonkinesigenic_dyskinesia dbr:Parry–Romberg_syndrome dbr:Smith–Magenis_syndrome dbr:Saethre–Chotzen_syndrome dbr:Barth_syndrome dbr:Bartter_syndrome dbr:Behçet's_disease dbr:Biemond_syndrome dbr:Biotinidase_deficiency dbr:Birt–Hogg–Dubé_syndrome dbr:Dementia_with_Lewy_bodies dbr:Anophthalmia dbr:Anterior_segment_mesenchymal_dysgenesis dbr:Anticipation_(genetics) dbr:Apert_syndrome dbr:Apparent_mineralocorticoid_excess_syndrome dbr:Arachnodactyly dbr:Arakawa's_syndrome_II dbr:Holt–Oram_syndrome dbr:Homocystinuria dbr:Huntington's_disease dbr:Hurler–Scheie_syndrome dbr:Hyaluronidase_deficiency dbr:Hyperammonemia dbr:Hyperekplexia dbr:Hyperimmunoglobulin_E_syndrome dbr:Hypohidrotic_ectodermal_dysplasia dbr:Hypokalemic_periodic_paralysis dbr:Hypophosphatasia dbr:Beta-mannosidosis dbr:Beta_thalassemia dbr:Bethlem_myopathy dbr:Arrhythmogenic_right_ventricular_dysplasia dbr:Patau_syndrome dbr:Pelger–Huet_anomaly dbr:Peutz–Jeghers_syndrome dbr:Peyronie's_disease dbr:Ring_18 dbr:Currarino_syndrome dbr:Cystinuria dbr:D-Glyceric_acidemia dbr:Ullrich_congenital_muscular_dystrophy dbr:Usher_syndrome dbr:CADASIL_syndrome dbr:Van_der_Woude_syndrome dbr:Variegate_porphyria dbr:Von_Hippel–Lindau_disease dbr:Von_Willebrand_disease dbr:De_Barsy_syndrome dbr:Degenerative_suspensory_ligament_desmitis dbr:Dejerine–Sottas_disease dbr:Desmin-related_myofibrillar_myopathy dbr:Donnai–Barrow_syndrome dbr:Donohue_syndrome dbr:Dopamine-responsive_dystonia dbr:Down_syndrome dbr:Dunnigan_familial_partial_lipodystrophy dbr:Inborn_errors_of_steroid_metabolism dbr:Incontinentia_pigmenti_achromians dbr:Infantile_neuronal_ceroid_lipofuscinosis dbr:Iniencephaly dbr:Jacobsen_syndrome dbr:Johanson–Blizzard_syndrome dbr:Leucism dbr:Leukodystrophy dbr:Lev's_disease dbr:Lhermitte–Duclos_disease dbr:Liddle's_syndrome dbr:Pearson_syndrome dbr:Pelizaeus–Merzbacher_disease dbr:Pendred_syndrome dbr:Steatosis dbr:Shaker_gene dbr:Reparagen dbr:Roberts_syndrome dbr:Congenital_insensitivity_to_pain dbr:Congenital_nephrotic_syndrome dbr:Copy-number_variation dbr:Cowden_syndrome dbr:Craniosynostosis dbr:Creutzfeldt–Jakob_disease dbr:Crigler–Najjar_syndrome dbr:Crohn's_disease dbr:Crouzon_syndrome dbr:Analbuminaemia dbr:Andersen–Tawil_syndrome dbr:Maturity_onset_diabetes_of_the_young dbr:Meckel_syndrome dbr:Menkes_disease dbr:Cherubism dbr:Erythromelalgia dbr:Erythropoietic_porphyria dbr:Erythropoietic_protoporphyria dbr:Genodermatosis dbr:Norrie_disease dbr:Ollier_disease dbr:Ondine's_curse dbr:Sakati–Nyhan–Tisdale_syndrome dbr:Online_Mendelian_Inheritance_in_Man dbr:Pallister–Killian_syndrome dbr:Simpson–Golabi–Behmel_syndrome dbr:X-linked_reticulate_pigmentary_disorder dbr:XMEN_disease dbr:PHACES_Syndrome dbr:Robinow_syndrome dbr:RASopathy dbr:Seaver_Cassidy_syndrome dbr:Chromosome_5q_deletion_syndrome dbr:Chronic_granulomatous_disease dbr:Citrullinemia dbr:Cockayne_syndrome dbr:Coeliac_disease dbr:Ehlers–Danlos_syndrome dbr:Ellis–van_Creveld_syndrome dbr:Emery–Dreifuss_muscular_dystrophy dbr:Epidermodysplasia_verruciformis dbr:Epidermolysis_bullosa_simplex dbr:Frontotemporal_dementia dbr:GJB2 dbr:Gardner's_syndrome dbr:Gaucher's_disease dbr:Generalized_epilepsy_with_febrile_seizures_plus dbr:Genetic_carrier dbr:Gilbert's_syndrome dbr:Glanzmann's_thrombasthenia dbr:Glycogen_storage_disease_type_I dbr:Glycogen_storage_disease_type_II dbr:Glycogen_storage_disease_type_III dbr:Glycogen_storage_disease_type_IV dbr:Glycogen_storage_disease_type_XI dbr:Branchio-oculo-facial_syndrome dbr:Branchio-oto-renal_syndrome dbr:Morquio_syndrome dbr:Multiple_epiphyseal_dysplasia dbr:Nail–patella_syndrome dbr:Congenital_absence_of_the_vas_deferens dbr:Congenital_adrenal_hyperplasia dbr:Congenital_contractural_arachnodactyly dbr:Congenital_fibrosis_of_the_extraocular_muscles dbr:Congenital_hyperinsulinism dbr:Congenital_insensitivity_to_pain_with_anhidrosis dbr:Contiguous_gene_syndrome dbr:Corneal_dystrophy dbr:Creatine_transporter_defect dbr:Maroteaux–Lamy_syndrome dbr:RAS-associated_autoimmune_leukoproliferative_disorder dbr:Alpha_1-antitrypsin_deficiency dbr:Sotos_syndrome dbr:Watson_syndrome dbr:Osteopoikilosis dbr:Otodental_syndrome dbr:Androgen_insensitivity_syndrome dbr:Angelman_syndrome dbr:Antley–Bixler_syndrome dbr:Batten_disease dbr:Legg–Calvé–Perthes_disease dbr:Lesch–Nyhan_syndrome dbr:Leukoencephalopathy_with_vanishing_white_matter dbr:Lipodystrophy dbr:Lissencephaly dbr:Loeys–Dietz_syndrome dbr:Lymphangioleiomyomatosis dbr:Bohring–Opitz_syndrome dbr:Choroideremia dbr:Sitosterolemia dbr:Smith–Lemli–Opitz_syndrome dbr:Steatocystoma_multiplex dbr:Stickler_syndrome dbr:Cleidocranial_dysostosis dbr:Coloboma dbr:Dent's_disease dbr:Dentinogenesis_imperfecta dbr:Denys–Drash_syndrome dbr:Emanuel_syndrome dbr:Feingold_syndrome dbr:Fraser_syndrome dbr:Friedreich's_ataxia dbr:Frontotemporal_lobar_degeneration dbr:Fucosidosis dbr:Fukuyama_congenital_muscular_dystrophy dbr:Fumarase_deficiency dbr:Club_foot dbr:Haemophilia_B dbr:Hagemoser–Weinstein–Bresnick_syndrome dbr:Hailey–Hailey_disease dbr:Hallermann–Streiff_syndrome dbr:De_Vivo_disease dbr:Joubert_syndrome dbr:Pachyonychia_congenita dbr:Papillon–Lefèvre_syndrome dbr:Paroxysmal_nocturnal_hemoglobinuria dbr:Pervasive_developmental_disorder dbr:Pfeiffer_syndrome dbr:Philadelphia_chromosome dbr:Poland_syndrome dbr:Porphyria_cutanea_tarda dbr:Primary_immunodeficiency dbr:Progeroid_syndromes dbr:Progressive_supranuclear_palsy dbr:Stargardt_disease dbr:Sturge–Weber_syndrome dbr:Treacher_Collins_syndrome dbr:Marker_chromosome dbr:May–Hegglin_anomaly dbr:McCune–Albright_syndrome dbr:McKusick–Kaufman_syndrome dbr:Medical_genetics dbr:Microcephaly_lymphoedema_chorioretinal_dysplasia dbr:Microspherophakia dbr:Microvillous_inclusion_disease dbr:Pitt–Hopkins_syndrome dbr:Yim–Ebbin_syndrome dbr:Spherocytosis dbr:Trimethylaminuria dbr:Autoimmune_lymphoproliferative_syndrome dbr:Autosomal_dominant_nocturnal_frontal_lobe_epilepsy dbr:Autosomal_dominant_polycystic_kidney_disease dbr:Axenfeld_syndrome dbr:6-Pyruvoyltetrahydropterin_synthase_deficiency dbr:Activated_protein_C_resistance dbr:Acute_intermittent_porphyria dbr:Adenosine_deaminase_deficiency dbr:Adermatoglyphia dbr:Adiposis_dolorosa dbr:Aicardi_syndrome dbr:Aicardi–Goutières_syndrome dbr:Thyroid_hormone_resistance dbr:Thyrotoxic_periodic_paralysis dbr:Tourette_syndrome dbr:Trichothiodystrophy dbr:Triple_X_syndrome dbr:Tuberous_sclerosis dbr:Turner_syndrome dbr:Weill–Marchesani_syndrome dbr:Wilms'_tumor dbr:Wilson's_disease dbr:Wiskott–Aldrich_syndrome dbr:Distal_18q- dbr:Distal_spinal_muscular_atrophy_type_2 dbr:Dubowitz_syndrome dbr:Galactokinase_deficiency dbr:Galactosialidosis dbr:Galloway_Mowat_syndrome dbr:Gangliosidosis dbr:Gitelman_syndrome dbr:Cornelia_de_Lange_Syndrome dbr:Cortical_dysplasia dbr:Hartnup_disease dbr:Hay–Wells_syndrome dbr:Jesse_Gelsinger dbr:Fatal_familial_insomnia dbr:Laminopathy dbr:Langer–Giedion_syndrome dbr:Leber's_hereditary_optic_neuropathy

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