glycogen storage disease type V

calbc-group:ANAT, calbc-group:CHEM, calbc-group:CONC, calbc-group:DISO, calbc-group:GENE, calbc-group:PHEN, calbc-group:PROC

MSH: Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise.,CSP: glycogenosis due to muscle phosphorylase deficiency; characterized by painful cramps following sustained exercise.,NCI: An autosomal recessive inherited type of glycogen storage disease caused by deficiency of myophosphorylase. It results in myalgias, muscle cramping and stiffness, and exercise intolerance.

umls-concept:C0017919

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