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Purine Nucleoside Phosphorylase Deficiency MeSH Supplementary Concept Data 2024


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
Registry Number
0
Heading Mapped to
*Primary Immunodeficiency Diseases
Purine-Nucleoside Phosphorylase / *deficiency
*Purine-Pyrimidine Metabolism, Inborn Errors
Frequency
17
Note
mutation in purine nucleoside phosphorylase
Date of Entry
2012/11/05
Revision Date
2019/06/17
Purine Nucleoside Phosphorylase Deficiency Preferred
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