Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
MONDO:0014768Any CADASIL in which the cause of the disease is a mutation in the HTRA1 gene.
Also known as: CADASIL caused by mutation in HTRA1, CADASIL type 2, CADASIL2, HTRA1 CADASIL, cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
0 clinical trials for this condition and its sub-types.
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Broader categories
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)
Disease by body system or component
(0)
Disease by etiologic mechanism
(0)
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