Hypoxanthine guanine phosphoribosyltransferase partial deficiency

MONDO:0010299

Kelley-Seegmiller syndrome (KSS) is the mildest form of hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency, a hereditary disorder of purine metabolism, and is associated with uric acid overproduction (UAO) leading to urolithiasis, and early-onset gout.

Also known as: HPRT deficiency, grade I, HPRT partial deficiency, HPRT-related gout, HPRT-related hyperuricemia, HPRT1 partial deficiency, Kelley-Seegmiller syndrome, hyperuricemia, HRPT-related, X-linked recessive, hypoxanthine guanine phosphoribosyltransferase 1 partial deficiency

25 clinical trials for this condition and its sub-types.

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