Disease #05061 (WAS (Wiskott-Aldrich syndrome (WAS)), OMIM:301000)

Official abbreviation WAS
Name Wiskott-Aldrich syndrome (WAS)
OMIM ID 301000
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene WAS
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 11:00:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00411262 - - - M yes Turkey - 00y02m - - - WAS Thrombocytopenia (HP:0001873), Intracranial hemorrhage (HP:0002170) - WAS 1 1 Aysel Tekmenuray-Unal
00464524 - - - M - - (not applicable) white - - - - WAS HP:0001873, HP:0001419, HP:0002721 - WAS 1 1 Marketa Wayhelova
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