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


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
Registry Number
0
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 Preferred
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