MeSH Browser

MeSH Supplementary: Thrombocytopenia 1
Unique ID: C564052
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564052
Entry Term(s): Thrombocytopenia, X-Linked; Thrombocytopenia, X-Linked, 1; X-Linked Thrombocytopenia
Registry Numbers: 0
Heading Mapped to: *Thrombocytopenia; *Genetic Diseases, X-Linked
Frequency: 32
Note: Hereditary, X-linked thrombocytopenia caused by mutations in the WISKOTT-ALDRICH SYNDROME PROTEIN (WAS) gene. OMIM: 313900
Date of Entry: 2012/11/05
Revision Date: 2016/09/29

Concept UI: M0564352
Registry Numbers: 0
Terms: Thrombocytopenia 1 Preferred Term
Term UI T804133
Date11/15/2011
LexicalTag NON
ThesaurusID; Thrombocytopenia, X-Linked
Term UI T804134
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Thrombocytopenia, X-Linked, 1
Term UI T804135
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); X-Linked Thrombocytopenia
Term UI T842782
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014)

Thrombocytopenia 1 MeSH Supplementary Concept Data 2025