MeSH Browser

MeSH Supplementary: Lymphoproliferative Syndrome, X-Linked, 2
Unique ID: C564469
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564469
Entry Term(s): XIAP Deficiency
Registry Numbers: 0
Heading Mapped to: *Lymphoproliferative Disorders; *Genetic Diseases, X-Linked
Frequency: 42
Note: mutation in XIAP
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Lymphoproliferative Syndrome, X-Linked, 2 MeSH Supplementary Concept Data 2025