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CPT deficiency, hepatic, type I (medical condition): A very rare inherited deficiency of a particular enzyme (Carnitine palmitoyl transferase I) prevents fatty acids being transported to the part of the cell that converts it to energy.
See also:
Carnitine palmitoyl transferase 1 deficiency:
»Introduction: Carnitine palmitoyl transferase 1 deficiency
»Symptoms of Carnitine palmitoyl transferase 1 deficiency
»Treatments for Carnitine palmitoyl transferase 1 deficiency
These medical condition or symptom topics may be relevant to medical information for CPT deficiency, hepatic, type I:
CPT deficiency, hepatic, type I: Another name for Carnitine palmitoyl transferase 1 deficiency (or close medical condition association).
»Introduction: Carnitine palmitoyl transferase 1 deficiency
»Symptoms of Carnitine palmitoyl transferase 1 deficiency
»Treatments for Carnitine palmitoyl transferase 1 deficiency
Some of the symptoms of CPT deficiency, hepatic, type I incude:
Treatments for CPT deficiency, hepatic, type I (Carnitine palmitoyl transferase 1 deficiency) include:
Read more about treatments for CPT deficiency, hepatic, type I
Treatment of CPT deficiency, hepatic, type I: For more treatment information about CPT deficiency, hepatic, type I, see treatment of Carnitine palmitoyl transferase 1 deficiency (CPT deficiency, hepatic, type I)
These medical disease topics may be related to CPT deficiency, hepatic, type I:
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