Carnitine acetyltransferase deficiency
MONDO:0011642A 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.
Also known as: carnitine acetyltransferase deficiency, Acetyl-carnitine deficiency, CrAT, acetyl-carnitine deficiency
0 clinical trials for this condition and its sub-types, 0 tagged with Carnitine acetyltransferase deficiency itself.
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