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UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
G G0 G1 G2 G3 G4 GA GB GC GD GE GF GG GH GI GL GM GN GO GP GQ GR GS GT GU GV GW GX GY GZ G%
GL GL3 GL7 GLA GLE GLI GLL GLM GLN GLO GLP GLU GLV GLY

glycogen storage disease type VIII

[x-linked recessive hepatic glycogen storage disease resulting from lack of expression of phosphorylase-b-kinase activity; symptoms are relatively mild, hepatomegaly, increased liver glycogen, and decreased leukocyte phosphorylase are present; liver shrinkage occurs in response to glucagon. ( CSP )]
UMLS (CSP) C0017927
 
Disease or Syndrome
Relation/PAR: glycogen storage disease

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