Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal [Supplementary Concept]

mutation in CPT2

MeSH Unique ID: C563463

Heading Mapped to:

• Carnitine O-Palmitoyltransferase/deficiency
• Infant, Newborn, Diseases
• Mitochondrial Diseases

Entry Terms:

• CPT II Deficiency, Lethal Neonatal
• CPT2 Deficiency, Lethal Neonatal
• Carnitine Palmitoyltransferase II Deficiency, Neonatal
• Carnitine Palmitoyltransferase II Deficiency, Antenatal