Disease association ontology term - MONDO:0014768 - cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
Term summary
- ID
- MONDO:0014768
- Name
- cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
- Ontology or CV name
- Disease association
- Definition
- Any CADASIL in which the cause of the disease is a mutation in the HTRA1 gene.
