All diseases

OMIM ID
232500
OMIM term:
GLYCOGEN STORAGE DISEASE IV
Alternative terms:
GSD IV; GSD4
GLYCOGEN BRANCHING ENZYME DEFICIENCY
GBE1 DEFICIENCY
ANDERSEN DISEASE
BRANCHER DEFICIENCY
GLYCOGENOSIS IV
AMYLOPECTINOSIS
CIRRHOSIS, FAMILIAL, WITH DEPOSITION OF ABNORMAL GLYCOGEN GSD IV, CLASSIC HEPATIC, INCLUDED
GSD IV, NONPROGRESSIVE HEPATIC, INCLUDED
GSD IV, NEUROMUSCULAR FORM, FATAL PERINATAL, INCLUDED
GSD IV, NEUROMUSCULAR FORM, CONGENITAL, INCLUDED
GSD IV, NEUROMUSCULAR FORM, CHILDHOOD, INCLUDED
GSD IV, NEUROMUSCULAR FORM, ADULT, WITH ISOLATED MYOPATHY, INCLUDED
(∗) Location:
3p12.2  
(†) Associated OMIM genes:
GBE1  
(‡) Associated MGI genes:
Gbe1  

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