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DO Term : Lesch-Nyhan syndrome [DOID:1919] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A purine-pyrimidine metabolic disorder characterized by mental retardation, spastic cerebral palsy, choreoathetosis, uric acid urinary stones, and self-destructive biting of fingers and lips that has_material_basis_in mutation in the HPRT1 gene on chromosome Xq26.
  • synonyms:
  • ICD10CM:E79.1,
  • OMIM:300322,
  • 300322,
  • deficiency of IMP pyrophosphorylase,
  • UMLS_CUI:C0023374,
  • HPRT1 deficiency,
  • Lesch - Nyhan syndrome,
  • NCI:C61255,
  • hypoxanthine guanine phosphoribosyltransferase deficiency,
  • MESH:D007926,
  • Hypoxanthine-guanine-phosphoribosyltransferase deficiency,
  • SNOMEDCT_US_2023_03_01:190918000,
  • HG-PRT deficiency,
  • X-linked hyperuricemia,
  • Hypoxanthine-guanine phosphoribosyltransferase deficiency,
  • Complete hypoxanthine-guanine phosphoribosyltransferase deficiency
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