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Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy; CADASIL

Disease ID:1157
Name:Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy; CADASIL
Associated with:1 target
Synonyms
Hereditary multi-infarct dementia
Database Links
OMIM: 125310
Orphanet: ORPHA136

Targets

notch 3

Ligands

No ligand related data available for Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy; CADASIL