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Genetic disorders by system
Genetic disorders by system
Concept
http://dbpedia.org/resource/Category:Genetic_disorders_by_system
Amelogenesis imperfecta
Asperger syndrome
Color blindness
Familial thoracic aortic aneurysm
Hyper IgM syndrome
Microphthalmia
Muscular dystrophy
Osteopetrosis
Sideroblastic anemia
Spinal muscular atrophies
Vitiligo
Acorea, microphthalmia and cataract syndrome
CD25 deficiency
Congenital generalized lipodystrophy
Congenital myopathy
Reticular dysgenesis
Severe combined immunodeficiency
Severe combined immunodeficiency (non-human)
Spondylo-meta-epiphyseal dysplasia
Spondylocostal dysostosis
subject
Albinism
Cardiogenetic disorders
Genodermatoses
Haemophilia
Huntington's disease
Muscular dystrophy
Neurogenetic disorders
broader
Genetic disorders by system
Concept
http://dbpedia.org/resource/Category:Genetic_disorders_by_system
Wikipage page ID
29,889,834
http://www.w3.org/2001/XMLSchema#integer
Wikipage revision ID
740,368,165
http://www.w3.org/2001/XMLSchema#integer
type
Concept
label
Genetic disorders by system
@en
sameAs
Q6902503
Q6902503
broader
Genetic diseases and disorders
prefLabel
Genetic disorders by system
@en
wasDerivedFrom
Category:Genetic_disorders_by_system?oldid=740368165