carnitine palmitoyltransferase II deficiency
lipid metabolism disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria
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carnitine palmitoyltransferase II deficiency
Summary
carnitine palmitoyltransferase II deficiency is a rare disease[1]. It draws 64 Wikipedia views per month (rare_disease category, ranking #194 of 627).[2]
Key Facts
- carnitine palmitoyltransferase II deficiency's instance of is recorded as rare disease[3].
- carnitine palmitoyltransferase II deficiency's instance of is recorded as class of disease[4].
- carnitine palmitoyltransferase II deficiency's subclass of is recorded as lipid metabolism disorder[5].
- carnitine palmitoyltransferase II deficiency's MeSH descriptor ID is recorded as C535589[6].
- carnitine palmitoyltransferase II deficiency's OMIM ID is recorded as 255110[7].
- carnitine palmitoyltransferase II deficiency's OMIM ID is recorded as 600649[8].
- carnitine palmitoyltransferase II deficiency's OMIM ID is recorded as 608836[9].
- carnitine palmitoyltransferase II deficiency's DiseasesDB is recorded as 32534[10].
- carnitine palmitoyltransferase II deficiency's KEGG ID is recorded as H01982[11].
- carnitine palmitoyltransferase II deficiency's GeneReviews ID is recorded as NBK1253[12].
- carnitine palmitoyltransferase II deficiency's eMedicine ID is recorded as 942233[13].
- carnitine palmitoyltransferase II deficiency's Disease Ontology ID is recorded as DOID:0060235[14].
- carnitine palmitoyltransferase II deficiency's Orphanet ID is recorded as 157[15].
- carnitine palmitoyltransferase II deficiency's NCI Thesaurus ID is recorded as C114766[16].
- carnitine palmitoyltransferase II deficiency's health specialty is recorded as endocrinology[17].
- carnitine palmitoyltransferase II deficiency's genetic association is recorded as CPT2[18].
- carnitine palmitoyltransferase II deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060235[19].
- carnitine palmitoyltransferase II deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0060235[20].
- carnitine palmitoyltransferase II deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_157[21].
- carnitine palmitoyltransferase II deficiency's UMLS CUI is recorded as C1850734[22].
- carnitine palmitoyltransferase II deficiency's PatientsLikeMe condition ID is recorded as Carnitine-palmitoyltransferase-2-deficiency[23].
- carnitine palmitoyltransferase II deficiency's GARD rare disease ID is recorded as 1121[24].
- carnitine palmitoyltransferase II deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[25].
- carnitine palmitoyltransferase II deficiency's Microsoft Academic ID is recorded as 2781290377[26].
- carnitine palmitoyltransferase II deficiency's Genetics Home Reference Conditions ID is recorded as carnitine-palmitoyltransferase-ii-deficiency[27].
Why It Matters
carnitine palmitoyltransferase II deficiency draws 64 Wikipedia views per month (rare_disease category, ranking #194 of 627).[2] It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28] It is known by 5 alternative names across languages and contexts.[29]