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Carnitine Acetyltransferase Deficiency MeSH Supplementary Concept Data 2025


MeSH Supplementary
Carnitine Acetyltransferase Deficiency
Unique ID
C563249
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C563249
Heading Mapped to
*Ataxia
Carnitine O-Acetyltransferase / deficiency
*Confusion
*Metabolism, Inborn Errors
*Muscle Hypotonia
*Oculomotor Nerve Diseases
Frequency
0
Date of Entry
2012/11/05
Revision Date
2013/11/06
Carnitine Acetyltransferase Deficiency Preferred
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