All diseases

OMIM ID
125310
OMIM term:
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CADASIL
Alternative terms:
DEMENTIA, HEREDITARY MULTI-INFARCT TYPE
CASIL
(∗) Location:
19p13.12  
(†) Associated OMIM genes:
NOTCH3  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/59a25ob7