Cerebral 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.

Also known as CADASIL caused by mutation in HTRA1, CADASIL type 2, CADASIL2, cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2, HTRA1 CADASIL — per MONDO

Also identified as

• DOID 0111036 per MONDO
• OMIM 616779 per MONDO
• UMLS C4225211 per MONDO