glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form

Findings

No curated finding names glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Where it sits

A kind of

• glycogen storage disease due to glycogen branching enzyme deficiency

Resolves to: glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form

Also called

GBE deficiency, congenital neuromuscular formglycogen storage disease type 4, congenital neuromuscular formglycogen storage disease type IV, congenital neuromuscular formglycogenosis due to glycogen branching enzyme deficiency, congenital neuromuscular formglycogenosis type 4, congenital neuromuscular formglycogenosis type IV, congenital neuromuscular formGSD due to glycogen branching enzyme deficiency, congenital neuromuscular formGSD type 4, congenital neuromuscular formGSDIV, congenital neuromuscular form