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Possible Causes For Lesch-Nyhan syndrome - Causes

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List of current finding(s):

Metabolic, Storage Disorders
Lesch-Nyhan syndrome
Synonyms
Choreoathetosis Self Mutilation Hyperuricemia Syndrome, Choreoathetosis Self-Mutilation Hyperuricemia Syndrome, Choreoathetosis self-mutilation syndrome, Comp hypoxan-guan phosribo def, COMPLETE HGPRT DEFIC DIS, Complete HGPRT deficiency, Complete HGPRT Deficiency Disease, Complete hypoxanthine-guanine phosphoribosyltransferase def, Complete hypoxanthine-guanine phosphoribosyltransferase deficiency, DEFIC DIS COMPLETE HGPRT, DEFIC DIS HYPOXANTHINE PHOSPHORIBOSYL TRANSFERASE, Deficiency Disease Complete HGPRT, Deficiency Disease Hypoxanthine Phosphoribosyl Transferase, Deficiency Disease Hypoxanthine-Phosphoribosyl-Transferase, Deficiency Diseases Hypoxanthine-Phosphoribosyl-Transferase, deficiency hypoxanthine(-guanine)-phosphoribosyltransferase, Deficiency of guanine phosphoribosyltransferase, Deficiency of hypoxanthine phosphoribosyltransferase, Deficiency of hypoxanthine phosphoribosyltransferase (disorder), Deficiency of hypoxanthine-guanine phosphoribosyltransferase, Deficiency of IMP pyrophosphorylase, Disease Hypoxanthine-Phosphoribosyl-Transferase Deficiency, Disease Lesch-Nyhan, Diseases Hypoxanthine-Phosphoribosyl-Transferase Deficiency, HEREDITARY HYPERURICEMIA, HGPRT DEFIC DIS COMPLETE, HGPRT deficiency, HG-PRT deficiency, HGPRT Deficiency Disease Complete, HG-PRT deficiency syndrome, HPRT DEFICIENCY, HPRT DEFICIENCY COMPLETE, HPRT Hypoxanthine-guanine phosphoribosyltransferase deficiency, HPRT1 DEFICIENCY, HPRT-Hypoxa-guan phosribos def, HPRT-Hypoxanthine-guanine phosphoribosyltransferase defic, HYPERURICEMIA CHOREOATHETOSIS SELF-MUTILATION SYNDROME, Hypoxan-guan phosphoribosy def, HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1 DEFICIENCY, hypoxanthine guanine phosphoribosyltransferase deficiency, HYPOXANTHINE PHOSPHORIBOSYL TRANSFERASE DEFIC DIS, Hypoxanthine Phosphoribosyl Transferase Deficiency Disease, hypoxanthine phosphoribosyltransferse (HPRT) deficiency, hypoxanthine phosphoribosyltransferse deficiency, hypoxanthine(-guanine)-phosphoribosyltransferase deficiency, hypoxanthine-guanine phosphoribosyltransferase (HGPRT) deficiency, hypoxanthine-guanine phosphoribosyltransferase deficiency, Hypoxanthine-guanine phosphoribosyltransferase deficiency (disorder), Hypoxanthine-guanine-phosphoribosyltransferase deficiency, Hypoxanthine-guanine-phosphoribosyltransferase deficiency ((Lesch Nyhan syndrome)), Hypoxanthine-guanine-phosphoribosyltransferase deficiency syndrome, Hypoxanthine-Phosphoribosyl-Transferase Deficiency Disease, Hypoxanthine-Phosphoribosyl-Transferase Deficiency Diseases, JUVENILE GOUT CHOREOATHETOSIS MENTAL RETARDATION SYNDROME, juvenile hyperuricemia syndrome, LESCH NYHAN DIS, Lesch Nyhan Disease, Lesch Nyhan syndrome, Lesch-Nyhan, Lesch-Nyhan disease, Lesch-Nyhan syndrome (disorder), Lesch-Nyhan syndrome (LNS), LNS, NYHAN SYNDROME, primary hyperuricemia syndrome, Total HGPRT deficiency, Total hypoxanthine-guanine phosphoribosyl transferase deficiency, X-linked hyperuricaemia, X-linked hyperuricemia, X-linked hyperuricemia (disorder), X-linked primary hyperuricemia, X-linked uric aciduria enzyme defect
Definition
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Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)
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