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disease > genetic disease > hereditary disease > CADASIL syndrome
disease > cardiovascular disease > vascular disease > arterial disease > CADASIL syndrome
disease > cardiovascular disease > vascular dementia > CADASIL syndrome
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > cerebrovascular disease > vascular dementia > CADASIL syndrome
... > disease > cardiovascular disease > vascular disease > cerebrovascular disease > vascular dementia > CADASIL syndrome
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > dementia > vascular dementia > CADASIL syndrome
disease > degenerative disease > dementia > vascular dementia > CADASIL syndrome

Terme préférentiel

CADASIL syndrome  

Définition

  • CADASIL or CADASIL syndrome, involving cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, is the most common form of hereditary stroke disorder, and is thought to be caused by mutations of the Notch 3 gene on chromosome 19. The disease belongs to a family of disorders called the leukodystrophies. (Wikipedia)

Concept générique

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-BR24NLLD-X

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