beta-ketothiolase deficiency
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beta-ketothiolase deficiency
Summary
beta-ketothiolase deficiency is a designated intractable/rare disease[1]. It draws 27 Wikipedia views per month (designated_intractable_rare_disease category, ranking #155 of 201).[2]
Key Facts
- beta-ketothiolase deficiency's instance of is recorded as designated intractable/rare disease[3].
- beta-ketothiolase deficiency's instance of is recorded as rare disease[4].
- beta-ketothiolase deficiency's instance of is recorded as class of disease[5].
- beta-ketothiolase deficiency is a type of autosomal recessive disease[6].
- beta-ketothiolase deficiency is a type of congenital disorder of amino acid metabolism[7].
- beta-ketothiolase deficiency is a type of inborn disorder of ketolysis[8].
- beta-ketothiolase deficiency is a type of classic organic aciduria[9].
- beta-ketothiolase deficiency is a type of amino acid metabolic disorder[10].
- beta-ketothiolase deficiency's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/5443[11].
- beta-ketothiolase deficiency's NCI Thesaurus ID is recorded as C98841[12].
- beta-ketothiolase deficiency's genetic association is recorded as ACAT1[13].
- beta-ketothiolase deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14723[14].
- beta-ketothiolase deficiency's exact match is recorded as http://identifiers.org/doid/DOID:14723[15].
- beta-ketothiolase deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_134[16].
- beta-ketothiolase deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
beta-ketothiolase deficiency draws 27 Wikipedia views per month (designated_intractable_rare_disease category, ranking #155 of 201).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[18] It is known by 24 alternative names across languages and contexts.[19]