Disease #00536 (angiopathy, amyloid, cerebral, CST3-related (Icelandic type, amyloidosis type VI), OMIM:105150)

Official abbreviation -
Name angiopathy, amyloid, cerebral, CST3-related (Icelandic type, amyloidosis type VI)
OMIM ID 105150
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CST3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-23 23:07:15 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00019986 - PubMed: Palsdottir 1988, Journal: Palsdottir 1988 8 families, 22 patients - no Iceland - - - - - angiopathy, amyloid, cerebral, CST3-related (Icelandic type, amyloidosis type VI) see paper; cerebral hemorrhage, paralysis CST3 CST3 1 22 Johan den Dunnen
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