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Up to: Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyl transferase II deficiency, myopathic form
The myopathic form of carnitine palmitoyltransferase II (CPT II) deficiency, an inherited metabolic disorder that affects mitochondrial oxidation of long chain fatty acids (LCFA), is the most common and the least severe form of CPT II deficiency.
This condition has no sub-types.