carnitine palmitoyltransferase II deficiency (Q2033861)
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lipid metabolism disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria
- CPT-II
- infantile carnitine palmitoyltransferase II deficiency
- late-onset carnitine palmitoyltransferase II deficiency
- lethal neonatal carnitine palmitoyltransferase II deficiency
Language | Label | Description | Also known as |
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English | 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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Statements
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3 references
C114766
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Identifiers
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Sitelinks
Wikipedia(9 entries)
- arwiki عوز إنزيم كارنيتين بالميتويل ترانسفيراز 2
- bswiki Nedostatak karnitin-palmitoiltransferaze II
- dewiki CPT 2-Mangel
- enwiki Carnitine palmitoyltransferase II deficiency
- eswiki Deficiencia de carnitina palmitoiltransferasa tipo II
- frwiki Déficit en carnitine palmitoyltransférase II
- mkwiki Недостаток на карнитин палмитоилтрансфераза II
- orwiki କାର୍ନିଟାଇନ ପାମିଟଏଲଟ୍ରାନ୍ସଫରେଜ ୨ ଅଭାବ
- svwiki CPT II-brist