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GENATLAS PHENOTYPE

last update : 6/07/2006

Symbol	HCHWAD
Location	21q21.3
Name	hereditary cerebral hemorrhage with amyloidosis, Dutch type
Other name(s)	amyloidosis VIb, late cerebral arterial
Corresponding gene	APP
Genetic determination	autosomal dominant
Function/system disorder	neurology
Type	disease

Gene product

Name	amyloid beta (A4) protein deposit

Remark(s)