| Label | Id | |
|---|---|---|
| CADASIL2 | 14768 | |
| CADASIL 2 | 14768 | |
| HTRA1 CADASIL | 14768 | |
| CADASIL type 2 | 14768 | |
| cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 | 14768 | |
| cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2; CADASIL2 | http://purl.obolibrary.org/obo/MONDO_0014768 | |
| CADASIL caused by mutation in HTRA1 | 14768 | |
| autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2 | 14768 |