glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form

Findings

No curated finding names glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic 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, childhood combined hepatic and myopathic form

Also called

GBE deficiency, childhood combined hepatic and myopathic formglycogen storage disease type 4, childhood combined hepatic and myopathic formglycogen storage disease type IV, childhood combined hepatic and myopathic formglycogenosis due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic formglycogenosis type 4, childhood combined hepatic and myopathic formglycogenosis type IV, childhood combined hepatic and myopathic formGSD due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic formGSD type 4, childhood combined hepatic and myopathic formGSDIV, childhood combined hepatic and myopathic form