Kelley-Seegmiller syndrome (Q97744)
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Kelley-Seegmiller syndrome is the mildest form of hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency, a hereditary disorder of purine metabolism, and is associated with uric acid overproduction leading to urolithiasis, and early-onset gout.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1094084865 |
||
| English | Kelley-Seegmiller syndrome |
Kelley-Seegmiller syndrome is the mildest form of hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency, a hereditary disorder of purine metabolism, and is associated with uric acid overproduction leading to urolithiasis, and early-onset gout. |
Statements
CID11:ID_1094084865
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dki-india-ID_1094084865
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Concluído
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15 August 2026
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