All diseases

OMIM ID
605714
OMIM term:
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
Alternative terms:
AMYLOIDOSIS, CEREBROARTERIAL, APP-RELATED
AMYLOIDOSIS, HEREDITARY, WITH CEREBRAL HEMORRHAGE, DUTCH VARIANT; HCHWAD
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT
(∗) Location:
21q21.3  
(†) Associated OMIM genes:
APP  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/4px75ind