Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1
MONDO:0000914A CADASIL characterized by migraine, strokes, and white matter lesions that has material basis in heterozygous mutation in the NOTCH3 gene on chromosome 19p13.
Also known as: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, CADASIL, CADASIL syndrome, CADASIL type 1, CADASIL1, CASIL, autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1, cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1
17 clinical trials for this condition and its sub-types.
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Cardiovascular disorder
(1051)
Disease
(680)
Hereditary disease
(176)
Vascular disorder
(135)
Syndromic disease
(25)
Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy
(14)
Human disease
(14)
Disease of genetic or genomic mechanism
(2)
Autosomal dominant disease
(0)
Autosomal genetic disease
(0)