Disease #02562 (Cerebral amyloid angiopathy, APP-related, OMIM:605714)

Official abbreviation -
Name Cerebral amyloid angiopathy, APP-related
OMIM ID 605714
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease -
Associated with 1 gene APP
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00148875 - PubMed: Levy E 1990 PubMed: Van Broeckhoven C 1990 PubMed: Fernandez-Madrid I 1991 - - - Netherlands white 48y - - - Cerebral amyloid angiopathy, APP-related - APP APP 1 1 Marc Cruts
00148876 - PubMed: Levy E 1990 PubMed: Van Broeckhoven C 1990 - - - Netherlands white 67y - - - Cerebral amyloid angiopathy, APP-related - APP APP 1 1 Marc Cruts
00148877 - PubMed: Levy E 1990 - - - Netherlands white - - - - Cerebral amyloid angiopathy, APP-related - APP APP 1 1 Marc Cruts
00148878 - PubMed: Levy E 1990 - - - Netherlands white - - - - Cerebral amyloid angiopathy, APP-related - APP APP 1 1 Marc Cruts
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