(Q2033861)

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

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit