Structured Summary
Abstract
Dysfunctions in the metabolism of PURINES or PYRIMIDINES resulting from inborn genetic mutations that are inherited or acquired in utero.
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Classification
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MeSH Record
Synonyms
2 entry terms
- Purine Pyrimidine Metabolism, Inborn Errors
- Purine-Pyrimidine Metabolism, Inborn Errors
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
coordinate with specific purine /metab or pyrimidine /metab
MeSH Record
History Note
65
MeSH Hierarchy
Tree Numbers
MeSH Record
NLM Classification
QU 265.5.P8
AMA Style
References
- National Library of Medicine. Inborn Errors Purine-Pyrimidine Metabolism. Medical Subject Headings (MeSH). 2026. Unique ID D011686. http://id.nlm.nih.gov/mesh/2026/D011686
- Inborn Errors Purine-Pyrimidine Metabolism. In: Wikipedia. https://en.wikipedia.org/wiki/Inborn_errors_of_purine%E2%80%93pyrimidine_metabolism
- Inborn Errors Purine-Pyrimidine Metabolism. In: Wikidata. https://www.wikidata.org/wiki/Q3281375