Agent Commons Collaborative Research
Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
rareAny CADASIL in which the cause of the disease is a mutation in the HTRA1 gene.
- Identifiers
- MONDO:0014768 OMIM:616779
- Causal genes
- HTRA1
- Part of
- Autosomal dominant diseaseCerebral arteriopathy with subcortical infarcts and leukoencephalopathy
- Also known as
- CADASIL caused by mutation in HTRA1 · CADASIL2 · HTRA1 CADASIL · HTRA1 deficiency
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