MeSH Browser

MeSH Heading: Purine-Pyrimidine Metabolism, Inborn Errors
Tree Number(s): C16.320.565.798; C18.452.648.798
Unique ID: D011686
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D011686
Annotation: coordinate with specific purine /‌metab or pyrimidine /‌metab
Scope Note: Dysfunctions in the metabolism of PURINES or PYRIMIDINES resulting from inborn genetic mutations that are inherited or acquired in utero.
Entry Version: PP METAB INBORN ERR
Entry Term(s): Purine Pyrimidine Metabolism, Inborn Errors
NLM Classification #: QU 265.5.P8
Public MeSH Note: 65
History Note: 65
Date Established: 1965/01/01
Date of Entry: 1999/01/01
Revision Date: 2016/07/06

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Purine-Pyrimidine Metabolism, Inborn Errors MeSH Descriptor Data 2024