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About:
http://dbpedia.org/class/yago/AutosomalDominantDisease114162025
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
:wordnet_autosomal_dominant_disease_114162025
is
rdf:
type
of
dbr
:Camurati–Engelmann_disease
dbr
:Rubinstein–Taybi_syndrome
dbr
:MOMO_syndrome
dbr
:Multiple_endocrine_neoplasia
dbr
:Metachondromatosis
dbr
:Saethre–Chotzen_syndrome
dbr
:Birt–Hogg–Dubé_syndrome
dbr
:Dermatopathia_pigmentosa_reticularis
dbr
:Arakawa's_syndrome_II
dbr
:Holt–Oram_syndrome
dbr
:Huntington's_disease
dbr
:Bethlem_myopathy
dbr
:Pelger–Huet_anomaly
dbr
:Peutz–Jeghers_syndrome
dbr
:Currarino_syndrome
dbr
:Variegate_porphyria
dbr
:Vitelliform_macular_dystrophy
dbr
:Von_Hippel–Lindau_disease
dbr
:Von_Willebrand_disease
dbr
:Dysfibrinogenemia
dbr
:Liddle's_syndrome
dbr
:Singleton_Merten_syndrome
dbr
:Medullary_cystic_kidney_disease
dbr
:RASopathy
dbr
:Gardner's_syndrome
dbr
:Gillespie_syndrome
dbr
:Branchio-oto-renal_syndrome
dbr
:Nail–patella_syndrome
dbr
:Congenital_distal_spinal_muscular_atrophy
dbr
:Congenital_stromal_corneal_dystrophy
dbr
:Marshall_syndrome
dbr
:Aromatase_excess_syndrome
dbr
:Stickler_syndrome
dbr
:Feingold_syndrome
dbr
:Felty's_syndrome
dbr
:Hajdu–Cheney_syndrome
dbr
:De_Vivo_disease
dbr
:Keratolytic_winter_erythema
dbr
:Pachyonychia_congenita
dbr
:Piebaldism
dbr
:Popliteal_pterygium_syndrome
dbr
:Porphyria_cutanea_tarda
dbr
:Spinal_muscular_atrophy_with_lower_extremity_predominance
dbr
:Treacher_Collins_syndrome
dbr
:Axenfeld_syndrome
dbr
:Acute_intermittent_porphyria
dbr
:Adermatoglyphia
dbr
:Tuberous_sclerosis
dbr
:Hawkinsinuria
dbr
:Hay–Wells_syndrome
dbr
:Langer–Giedion_syndrome
dbr
:Kostmann_syndrome
dbr
:22q13_deletion_syndrome
dbr
:Darier's_disease
dbr
:Noonan_syndrome
dbr
:Central_core_disease
dbr
:Familial_atrial_fibrillation
dbr
:Familial_male-limited_precocious_puberty
dbr
:Flynn–Aird_syndrome
dbr
:Gray_platelet_syndrome
dbr
:Dentatorubral-pallidoluysian_atrophy
dbr
:Kniest_dysplasia
dbr
:Miller–Dieker_syndrome
dbr
:Naegeli–Franceschetti–Jadassohn_syndrome
dbr
:Schmitt_Gillenwater_Kelly_syndrome
dbr
:Short_QT_syndrome
dbr
:Hereditary_elliptocytosis
dbr
:Hereditary_hemorrhagic_telangiectasia
dbr
:Hereditary_mucoepithelial_dysplasia
dbr
:Costello_syndrome
dbr
:Hypoalphalipoproteinemia
dbr
:Timothy_syndrome
dbr
:Papillorenal_syndrome
dbr
:Transthyretin-related_hereditary_amyloidosis
dbr
:Acropectoral_syndrome
dbr
:Albright's_hereditary_osteodystrophy
dbr
:Larsen_syndrome
dbr
:Collagen_disease
dbr
:Hereditary_spherocytosis
dbr
:Jackson–Weiss_syndrome
dbr
:Tietz_syndrome
dbr
:Worth_syndrome
dbr
:Reis–Bucklers_corneal_dystrophy
dbr
:DiGeorge_syndrome
dbr
:Autosomal_dominant_cerebellar_ataxia
dbr
:Marfan_syndrome
dbr
:Boomerang_dysplasia
dbr
:Buschke–Ollendorff_syndrome
dbr
:Spinocerebellar_ataxia
dbr
:Greig_cephalopolysyndactyly_syndrome
dbr
:Multiple_endocrine_neoplasia_type_2
dbr
:Spinocerebellar_ataxia_type_6
dbr
:WHIM_syndrome
dbr
:White_sponge_nevus
dbr
:Roussy–Lévy_syndrome
dbr
:Zori–Stalker–Williams_syndrome
dbr
:Zimmermann–Laband_syndrome
dbr
:Platyspondylic_lethal_skeletal_dysplasia,_Torrance_type
dbr
:Rosselli–Gulienetti_syndrome
dbr
:Multiple_endocrine_neoplasia_type_2b
dbr
:Myelokathexis
dbr
:Wallis–Zieff–Goldblatt_syndrome
dbr
:Monilethrix
dbr
:Multiple_endocrine_neoplasia_type_1
dbr
:Upington_disease
dbr
:Zaspopathy
dbr
:Spondyloperipheral_dysplasia
dbr
:Pallister–Hall_syndrome
dbr
:Romano–Ward_syndrome
dbr
:Spondyloepiphyseal_dysplasia_congenita
dbr
:PAPA_syndrome
dbr
:Parastremmatic_dwarfism
dbr
:Spondyloepimetaphyseal_dysplasia,_Strudwick_type
is
rdfs:
subClassOf
of
yago
:WikicatAutosomalDominantDisorders
yago
:MalignantHyperthermia114157782
yago
:Neurofibromatosis114158179
yago
:OsteogenesisImperfecta114158424
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