MeSH Browser

MeSH Supplementary: Purine Nucleoside Phosphorylase Deficiency
Unique ID: C562587
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562587
Entry Term(s): Nucleoside Phosphorylase Deficiency; PNP Deficiency
Heading Mapped to: Purine-Nucleoside Phosphorylase / deficiency; *Purine-Pyrimidine Metabolism, Inborn Errors; *Primary Immunodeficiency Diseases
Frequency: 17
Note: mutation in purine nucleoside phosphorylase
Date of Entry: 2012/11/05
Revision Date: 2019/06/17

Purine Nucleoside Phosphorylase Deficiency MeSH Supplementary Concept Data 2024