MeSH Browser

MeSH Supplementary: Carnitine Palmitoyltransferase II Deficiency, Late-Onset
Unique ID: C563461
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563461
Entry Term(s): CPT II Deficiency, Myopathic; CPT2 Deficiency, Late-Onset; Carnitine Palmitoyltransferase II Deficiency, Adult-Onset; Carnitine Palmitoyltransferase II Deficiency, Myopathic
Heading Mapped to: Carnitine O-Palmitoyltransferase / deficiency; *Lipid Metabolism, Inborn Errors; *Muscular Diseases; *Mitochondrial Diseases
Frequency: 5
Note: PROM mutation in carnitine palmitoyltransferase II
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Carnitine Palmitoyltransferase II Deficiency, Late-Onset MeSH Supplementary Concept Data 2024