glycogen storage disease
[any of a group of metabolic disorders characterized by excessive storage of glycogen. ( CSP )]
UMLS (CSP) C0017919- Disease or Syndrome
Relation/PAR: Carbohydrate Metabolism, Inborn Errors
enzyme deficiency
enzyme deficiency
Relation/CHD: G6PD deficiency
acid maltase deficiency
amylo 1,6 glucosidase deficiency
amylopectinosis
glycogen storage disease type V
glycogen storage disease type VI
glycogen storage disease type VII
glycogen storage disease type VIII
G6PD deficiency
acid maltase deficiency
amylo 1,6 glucosidase deficiency
amylopectinosis
glycogen storage disease type V
glycogen storage disease type VI
glycogen storage disease type VII
glycogen storage disease type VIII
acid maltase deficiency
amylo 1,6 glucosidase deficiency
amylopectinosis
glycogen storage disease type V
glycogen storage disease type VI
glycogen storage disease type VII
glycogen storage disease type VIII
G6PD deficiency
acid maltase deficiency
amylo 1,6 glucosidase deficiency
amylopectinosis
glycogen storage disease type V
glycogen storage disease type VI
glycogen storage disease type VII
glycogen storage disease type VIII
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