carnitine palmitoyltransferase II deficiency (Q2033861)

From Wikidata
Jump to navigation Jump to search
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
edit
Language Label Description Also known as
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
  • CPT-II
  • infantile carnitine palmitoyltransferase II deficiency
  • late-onset carnitine palmitoyltransferase II deficiency
  • lethal neonatal carnitine palmitoyltransferase II deficiency

Statements

Identifiers