DISEASES

Disease-gene associations mined from literature

Human genes for CADASIL

CADASIL [DOID:13945]

A leukodystrophy characterized by recurrent subcortical ischemic stroke and cognitive impairment.

Synonyms:  CADASIL,  DOID:13945,  cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy,  hereditary multi-infarct dementia,  hereditary multiinfarct dementia ...