Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2

MONDO:0014768

Any 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

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