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Dictionary » Cori type I glycogenosis
 

Cori type I glycogenosis

Introduction: Cori type I glycogenosis

Description of Cori type I glycogenosis

Cori type I glycogenosis (medical condition): A genetic metabolic disorder involving a deficiency of the enzyme glucose-6-phosphatase which results in the accumulation of glycogen in various tissues. G6P is stored as glycogen until the body needs to convert it to a sugar and use it to create energy. The enzyme deficiency prevents the conversion and hence low blood sugar levels result.

See also:

Von Gierke disease IA:
  »Introduction: Von Gierke disease IA
  »Symptoms of Von Gierke disease IA

Cori type I glycogenosis: Related Topics

These medical condition or symptom topics may be relevant to medical information for Cori type I glycogenosis:

Cori type I glycogenosis as a Disease

Cori type I glycogenosis: Another name for Von Gierke disease IA (or close medical condition association).
  »Introduction: Von Gierke disease IA
  »Symptoms of Von Gierke disease IA

Symptoms of Cori type I glycogenosis (Von Gierke disease IA)

Some of the symptoms of Cori type I glycogenosis incude:

See full list of 27 symptoms of Cori type I glycogenosis (Von Gierke disease IA)

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