Disease #01423 (BSSA2 (Bernard-Soulier syndrome, type A2, autosomal dominant (BSSA-2)), OMIM:153670)

Official abbreviation BSSA2
Name Bernard-Soulier syndrome, type A2, autosomal dominant (BSSA-2)
OMIM ID 153670
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 GP1BA
Associated tissues -
Disease features autosomal dominant
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

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00306219 122 - - F - China - - - - - BSSA2 - GP1BA GP1BA 1 1 Sha Hong
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