About: http://dbpedia.org/class/yago/GeneticDisease114151139

Property	Value
rdfs:subClassOf	yago:Disease114070360
owl:equivalentClass	yago-res:wordnet_genetic_disease_114151139
owl:sameAs	yago:GeneticDisease114151139
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:Amelanism dbr:Amelogenesis_imperfecta dbr:Aminolevulinic_acid_dehydratase_deficiency_porphyria dbr:48,_XXXX dbr:49,_XXXXX dbr:5-alpha-reductase_deficiency dbr:Bazex–Dupré–Christol_syndrome dbr:Beckwith–Wiedemann_syndrome dbr:Behr_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:Melorheostosis dbr:Metachondromatosis dbr:Metachromatic_leukodystrophy dbr:Metageria dbr:Metaphyseal_dysplasia dbr:Morgagni_Stewart_Morel_syndrome dbr:Nephronophthisis dbr:Say_syndrome dbr:Omenn_syndrome dbr:Paroxysmal_nonkinesigenic_dyskinesia dbr:Parry–Romberg_syndrome dbr:Partial_monosomy_13q 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:Branchial_cleft_cyst dbr:Dementia_with_Lewy_bodies dbr:Dermatopathia_pigmentosa_reticularis dbr:Anophthalmia dbr:Anterior_segment_mesenchymal_dysgenesis dbr:Anticipation_(genetics) dbr:Apert_syndrome dbr:Aplasia_cutis_congenita 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:Hyperphenylalaninemia dbr:Hypohidrotic_ectodermal_dysplasia dbr:Hypokalemic_periodic_paralysis dbr:Hypophosphatasia dbr:Beta-mannosidosis dbr:Beta_thalassemia dbr:Bethlem_myopathy dbr:Bhaskar–Jagannathan_syndrome 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:DOOR_syndrome dbr:Ullrich_congenital_muscular_dystrophy dbr:Usher_syndrome dbr:CADASIL_syndrome dbr:Van_der_Woude_syndrome dbr:Variegate_porphyria dbr:Vitelliform_macular_dystrophy 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:Dysfibrinogenemia dbr:Inborn_errors_of_steroid_metabolism dbr:Incontinentia_pigmenti_achromians dbr:Infantile_neuronal_ceroid_lipofuscinosis dbr:Inherited_disorders_of_trafficking dbr:Iniencephaly dbr:Interleukin-1_receptor–associated_kinase_4_deficiency dbr:Jacobsen_syndrome dbr:Johanson–Blizzard_syndrome dbr:Lethal_white_syndrome dbr:Leucism dbr:Leukodystrophy dbr:Lev's_disease dbr:Lhermitte–Duclos_disease dbr:Liddle's_syndrome dbr:Rosenthal–Kloepfer_syndrome dbr:Pearson_syndrome dbr:Pelizaeus–Merzbacher_disease dbr:Pendred_syndrome dbr:Pentalogy_of_Cantrell dbr:Steatosis dbr:Shaker_gene dbr:Scalp–ear–nipple_syndrome dbr:Sickle_Cell_Anemia,_a_Molecular_Disease dbr:Reparagen dbr:Roberts_syndrome dbr:Singleton_Merten_syndrome dbr:Congenital_generalized_lipodystrophy 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:Aniridia_ataxia_renal_agenesis_psychomotor_retardation dbr:Maturity_onset_diabetes_of_the_young dbr:Meckel_syndrome dbr:Medullary_cystic_kidney_disease dbr:Menkes_disease dbr:Cherubism dbr:Erondu–Cymet_syndrome dbr:Erythrism 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:Serpentine_fibula-polycystic_kidney_syndrome dbr:Simpson–Golabi–Behmel_syndrome dbr:X-linked_reticulate_pigmentary_disorder dbr:XMEN_disease dbr:PHACES_Syndrome dbr:Vici_syndrome dbr:Spondylocostal_dysostosis dbr:Robinow_syndrome dbr:RASopathy dbr:Scott_syndrome 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:Gastroschisis dbr:Gaucher's_disease dbr:Generalized_epilepsy_with_febrile_seizures_plus dbr:Genetic_carrier dbr:Gilbert's_syndrome dbr:Gillespie_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_distal_spinal_muscular_atrophy dbr:Congenital_dyserythropoietic_anemia dbr:Congenital_dyserythropoietic_anemia_type_I dbr:Congenital_dyserythropoietic_anemia_type_II dbr:Congenital_dyserythropoietic_anemia_type_III dbr:Congenital_dyserythropoietic_anemia_type_IV dbr:Congenital_fibrosis_of_the_extraocular_muscles dbr:Congenital_hyperinsulinism dbr:Congenital_insensitivity_to_pain_with_anhidrosis dbr:Congenital_myopathy dbr:Congenital_stromal_corneal_dystrophy dbr:Contiguous_gene_syndrome dbr:Cooks_syndrome dbr:Corneal_dystrophy dbr:Creatine_transporter_defect dbr:Cronkhite–Canada_syndrome dbr:Cross_syndrome dbr:Crouzonodermoskeletal_syndrome dbr:Lachiewicz–Sibley_syndrome dbr:Maroteaux–Lamy_syndrome dbr:Marshall_syndrome dbr:Nullisomic 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:Aromatase_excess_syndrome dbr:Batten_disease dbr:Benjamin_syndrome dbr:Berdon_syndrome dbr:Legg–Calvé–Perthes_disease dbr:Lesch–Nyhan_syndrome dbr:Lethal_arthrogryposis_with_anterior_horn_cell_disease 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:Snatiation dbr:Steatocystoma_multiplex dbr:Stickler_syndrome dbr:Cleidocranial_dysostosis dbr:Coloboma dbr:Dent's_disease dbr:Dentinogenesis_imperfecta dbr:Denys–Drash_syndrome dbr:Zunich–Kaye_syndrome dbr:Emanuel_syndrome dbr:Fazio–Londe_disease dbr:Feingold_syndrome dbr:Felty's_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:Hajdu–Cheney_syndrome dbr:Hallermann–Streiff_syndrome dbr:Hemoglobin_Lepore_syndrome dbr:Hemoglobin_variants dbr:De_Vivo_disease dbr:Joubert_syndrome dbr:Keratolytic_winter_erythema dbr:Pachyonychia_congenita dbr:Papillon–Lefèvre_syndrome dbr:Paroxysmal_nocturnal_hemoglobinuria
is rdfs:subClassOf of	yago:Abetalipoproteinemia114151884 yago:Achondroplasia114121804 yago:AutosomalDominantDisease114162025 yago:AutosomalRecessiveDisease114162275 yago:CongenitalAfibrinogenemia114171492 yago:CongenitalMegacolon114156488 yago:CongenitalPancytopenia114164866 yago:Dwarfism114506403 yago:HepatolenticularDegeneration114569121 yago:Hyperbetalipoproteinemia114158594 yago:Ichthyosis114158997 yago:InbornErrorOfMetabolism114155834 yago:JuvenileAmauroticIdiocy114169128 yago:LactoseIntolerance114506656 yago:MapleSyrupUrineDisease114159887 yago:MonogenicDisorder114074877 yago:Mucopolysaccharidosis114157527 yago:MuscularDystrophy114160365 yago:NevoidElephantiasis114367797 yago:Oligodactyly114160665 yago:Oligodontia114160786 yago:Osteopetrosis114210119 yago:Otosclerosis114160903 yago:PolygenicDisorder114075199 yago:Porphyria114507651 yago:WikicatGeneticDisorders yago:WikicatGeneticDisordersByInheritance yago:WikicatGeneticDisordersByMechanism yago:WikicatGeneticDisordersBySystem yago:WikicatGeneticDisordersWithKnownGeneButNoKnownGeneFunction yago:WikicatGeneticDisordersWithNoOMIM yago:WikicatGeneticDisordersWithOMIMButNoGene yago:WikicatInheritedDisordersOfTrafficking