Summary Literature (0)

MIM:232500 - GLYCOGEN STORAGE DISEASE IV; GSD4

Xenbase Genes: gbe1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009292 - glycogen storage disease due to glycogen branching enzyme deficiency

MONDO:0017695 - glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form

MONDO:0017696 - glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form

MONDO:0017697 - glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form

MONDO:0017698 - glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form

MONDO:0017699 - glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form

MONDO:0017700 - glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form

MONDO:0017701 - glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form

Disease Ontology (DO):

DOID:2750 - glycogen storage disease IV