Lesch-Nyhan syndrome
rare genetic syndrome
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Lesch-Nyhan syndrome
Summary
Lesch-Nyhan syndrome is a rare disease[1]. It has Wikipedia articles in 20 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Lesch-Nyhan syndrome's instance of is recorded as rare disease[3].
- Lesch-Nyhan syndrome's instance of is recorded as class of disease[4].
- Michael Lesch is named after Lesch-Nyhan syndrome[5].
- William Nyhan is named after Lesch-Nyhan syndrome[6].
- Lesch-Nyhan syndrome is a type of inborn errors of purine–pyrimidine metabolism[7].
- Lesch-Nyhan syndrome is a type of X-linked recessive disease[8].
- Lesch-Nyhan syndrome is a type of hypoxanthine-guanine phosphoribosyltransferase deficiency[9].
- Lesch-Nyhan syndrome is a type of disease[10].
- Lesch-Nyhan syndrome's symptoms and signs is recorded as self-injury[11].
- Lesch-Nyhan syndrome's has cause is recorded as Hypoxanthine phosphoribosyltransferase 1[12].
- Lesch-Nyhan syndrome's NCI Thesaurus ID is recorded as C61255[13].
- Lesch-Nyhan syndrome's health specialty is recorded as endocrinology[14].
- Lesch-Nyhan syndrome's drug or therapy used for treatment is recorded as allopurinol[15].
- Lesch-Nyhan syndrome's genetic association is recorded as HPRT1[16].
- Lesch-Nyhan syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_1919[17].
- Lesch-Nyhan syndrome's exact match is recorded as http://identifiers.org/doid/DOID:1919[18].
- Lesch-Nyhan syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
Lesch-Nyhan syndrome has Wikipedia articles in 20 language editions, a strong signal of global cultural recognition.[2] It is known by 23 alternative names across languages and contexts.[20]