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GENATLAS PHENOTYPE

last update : 10/12/2008

Symbol	HMID
Location	19p13.12
Name	hereditary multi-infarct dementia
Corresponding gene	NOTCH3
Main clinical features	chronic familial vascular encephalopathy in Swedish family, with several hereditary small vessel diseases (SVDs) of the brain several differences in arteriosclerotic changes in both the grey and white matter in CADASIL and HMID
Genetic determination	autosomal dominant
Function/system disorder	cardiovascular
Type	disease

Remark(s)