Gout, HPRT-Related [Supplementary Concept]
mutation in HPRT; complete deficiency = Lesch-Nyhan Syndrome
Date introduced: November 5, 2012
MeSH Unique ID: C562583
Heading Mapped to:
Entry Terms:
- Kelley-Seegmiller Syndrome
- Hypoxanthine Guanine Phosphoribosyltransferase 1 Deficiency, Partial
- HPRT Deficiency, Partial
- HPRT1 Deficiency, Partial