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Carnitine acetyltransferase deficiency
A disease arising from a defect of carnitine acetyltransferase causing disruption of whole-body glucose homeostasis and muscle-specific loss of function results in reduced metabolic control, which resembles the insulin resistant state.
- Identifiers
- MONDO:0011642 OMIM:606175
- Part of
- Hereditary disease
- Also known as
- Acetyl-carnitine deficiency · CrAT
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