Condition Article

Lesch-Nyhan syndrome

Medical Encyclopedia index entry — source-backed definition under review.

Disease Condition

Educational information only. This explains health information to discuss with a qualified clinician; it is not a diagnosis, prescription, or treatment. Medical Information & Safety.

Content remediation in progress. This concept remains catalogued with its terminology and classification. Its definition and full article are being prepared and reviewed; it is not presented as content-complete.

Concept record

Canonical title: Lesch-Nyhan syndrome
Alphabetical key: L
Category: Disease Condition
Content type: Condition Article
Other names, clinical names and abbreviations: Choreoathetosis Self-Mutilation Hyperuricemia Syndrome, Choreoathetosis Self-Mutilation Syndrome, Choreoathetosis Self-Mutilation Syndromes, Complete HGPRT Deficiency Disease, Complete HPRT Deficiencies, Complete HPRT Deficiency, Complete Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency, Deficiencies, Complete HPRT, Deficiencies, HGPRT, Deficiencies, Hypoxanthine Phosphoribosyltransferase, Deficiencies, Total HPRT, Deficiency, Complete HPRT, Deficiency Disease, Complete HGPRT, Deficiency Disease, Hypoxanthine-Phosphoribosyl-Transferase, Deficiency Diseases, Hypoxanthine-Phosphoribosyl-Transferase, Deficiency, HGPRT, Deficiency, Hypoxanthine Phosphoribosyltransferase, Deficiency of Guanine Phosphoribosyltransferase, Deficiency of Hypoxanthine Phosphoribosyltransferase, Deficiency, Total HPRT, Guanine Phosphoribosyltransferase Deficiencies, Guanine Phosphoribosyltransferase Deficiency, HGPRT Deficiencies, HGPRT Deficiency, HGPRT Deficiency Disease, Complete, HPRT Deficiencies, Complete, HPRT Deficiencies, Total, HPRT Deficiency, Complete, HPRT Deficiency, Total, Hyperuricemia Syndrome, Juvenile, Hyperuricemia Syndrome, Primary, Hyperuricemia Syndromes, Juvenile, Hyperuricemia Syndromes, Primary, Hyperuricemia, X-Linked, Hyperuricemia, X-Linked Primary, Hyperuricemias, X-Linked, Hyperuricemias, X-Linked Primary, Hypoxanthine Guanine Phosphoribosyltransferase 1 Deficiency, Hypoxanthine Guanine Phosphoribosyltransferase Deficiency, Hypoxanthine-Phosphoribosyl-Transferase Deficiency Disease, Hypoxanthine-Phosphoribosyl-Transferase Deficiency Diseases, Hypoxanthine Phosphoribosyltransferase Deficiencies, Hypoxanthine Phosphoribosyltransferase Deficiency, Juvenile Gout, Choreoathetosis, Mental Retardation Syndrome, Juvenile Hyperuricemia Syndrome, Juvenile Hyperuricemia Syndromes, Lesch-Nyhan Disease, Lesch-Nyhan Syndrome, Phosphoribosyltransferase Deficiencies, Guanine, Phosphoribosyltransferase Deficiencies, Hypoxanthine, Phosphoribosyltransferase Deficiency, Guanine, Phosphoribosyltransferase Deficiency, Hypoxanthine, Primary Hyperuricemia Syndrome, Primary Hyperuricemia Syndromes, Primary Hyperuricemia, X-Linked, Primary Hyperuricemias, X-Linked, Self-Mutilation Syndrome, Choreoathetosis, Self-Mutilation Syndromes, Choreoathetosis, Syndrome, Choreoathetosis Self-Mutilation, Syndrome, Juvenile Hyperuricemia, Syndrome, Primary Hyperuricemia, Syndromes, Choreoathetosis Self-Mutilation, Syndromes, Juvenile Hyperuricemia, Syndromes, Primary Hyperuricemia, Total HPRT Deficiencies, Total HPRT Deficiency, Total Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency, X-Linked Hyperuricemia, X-Linked Hyperuricemias, X-Linked Primary Hyperuricemia, X-Linked Primary Hyperuricemias
Article status: Medical Encyclopedia Index Entry — full article under review.

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