Carnitine Palmitoyltransferase II Deficiency, Late-Onset [Supplementary Concept]

PROM mutation in carnitine palmitoyltransferase II

MeSH Unique ID: C563461

Heading Mapped to:

• Carnitine O-Palmitoyltransferase/deficiency
• Lipid Metabolism, Inborn Errors
• Muscular Diseases
• Mitochondrial Diseases

Entry Terms:

• CPT2 Deficiency, Late-Onset
• CPT II Deficiency, Myopathic
• Carnitine Palmitoyltransferase II Deficiency, Myopathic
• Carnitine Palmitoyltransferase II Deficiency, Adult-Onset