/cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
Rare Disease
MONDO:0014768
Also Known As
CADASIL 2CADASIL caused by mutation in HTRA1CADASIL type 2CADASIL2HTRA1 CADASILautosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
Definition
Any CADASIL in which the cause of the disease is a mutation in the HTRA1 gene.
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