x

Search for a rare disease

* (*) mandatory field

Suggest an update

(*) Required fields.

Attention

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.

Captcha image

Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form

ORPHA:308621

  • Synonym(s):
    • GBE deficiency, progressive hepatic form
    • GSD due to glycogen branching enzyme deficiency, progressive hepatic form
    • GSD type 4, progressive hepatic form
    • GSDIV, progressive hepatic form
    • Glycogen storage disease type 4, progressive hepatic form
    • Glycogen storage disease type IV, progressive hepatic form
    • Glycogenosis due to glycogen branching enzyme deficiency, progressive hepatic form
    • Glycogenosis type 4, progressive hepatic form
    • Glycogenosis type IV, progressive hepatic form
  • Prevalence: -
  • Inheritance: -
  • Age of onset: -
  • ICD-10: E74.0
  • OMIM: 232500
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -

Additional information

Further information on this disease

Specialised Social Services

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.