MeSH Browser

MeSH Supplementary: Hyperuricemia, Infantile, with Abnormal Behavior and Normal Hypoxanthine Guanine Phosphoribosyltransferase
Unique ID: C565489
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565489
Registry Numbers: 0
Heading Mapped to: *Child Development Disorders, Pervasive; *Intellectual Disability; *Purine-Pyrimidine Metabolism, Inborn Errors; *Hyperuricemia
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2016/07/07

Hyperuricemia, Infantile, with Abnormal Behavior and Normal Hypoxanthine Guanine Phosphoribosyltransferase MeSH Supplementary Concept Data 2025