Search Ontology:
Human Disease
HRPT-related hyperuricemia
- Term ID
- DOID:0112127
- Synonyms
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- HPRT deficiency, grade I
- HPRT partial deficiency
- HPRT-related gout
- HPRT-related hyperuricemia
- HPRT1 partial deficiency
- hypoxanthine guanine phosphoribosyltransferase 1 partial deficiency
- hypoxanthine guanine phosphoribosyltransferase deficiency, grade I
- hypoxanthine guanine phosphoribosyltransferase partial deficiency
- Kelley-Seegmiller syndrome
- Definition
- A hyperuricemia characterized by excessive purine production often resulting in renal stones, uric acid nephropathy, and renal obstruction that has_material_basis_in hemizygous mutation in the HPRT1 gene on chromosome Xq26.2-q26.3. (2)
- References
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- MIM:300323
- ORDO:79233
- Ontology
- Human Disease ( DOID:0112127 )
- is a type of
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Genes Involved
Zebrafish Models