PEPCK mitochondrial (medical condition): A rare inherited disorder where deficiency of an enzyme (phosphoenolpyruvate carboxykinase-2) prevents fats and proteins being turned into glucose which causes various problems. In type 2 the deficiency occurs in the mitochondrial part of the cell which is the energy conversion organelle in the cell.
See also:
PEPCK 2 deficiency:
»Introduction: PEPCK 2 deficiency
»Symptoms of PEPCK 2 deficiency
These medical condition or symptom topics may be relevant to medical information for PEPCK mitochondrial:
PEPCK mitochondrial: Another name for PEPCK 2 deficiency (or close medical condition association).
»Introduction: PEPCK 2 deficiency
»Symptoms of PEPCK 2 deficiency
Some of the symptoms of PEPCK mitochondrial incude:
Read more about symptoms of PEPCK mitochondrial (PEPCK 2 deficiency)
These medical disease topics may be related to PEPCK mitochondrial:
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