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

0 clinical trials for this condition and its sub-types, 0 tagged with Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 itself.

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↑ Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (19)

Sub-types of Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2

CARASIL syndrome 0 trials

Including sub-types (0) Tagged with Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 (0)

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