Language

Home/Rare disease/Congenital myasthenic syndrome with glycosylation defect

Congenital myasthenic syndrome with glycosylation defect

ORPHA:353327· ICD-10 G70.2

Prevalence: Unknown
Inheritance: Autosomal recessive
Age of onset: Infancy, Neonatal

ICD-10 G70.2 →

EN DE FR CS TR PL IT UK ES NL PT ZH

Not medical advice. Consult a healthcare professional. This information is general reference based on public data and does not replace consultation with a doctor or pharmacist.

Source:

Orphanet — Orphanet Rare Disease Nomenclature (CC BY 4.0) [Source data]

Source: Orphanet (orpha.net) — used under CC BY 4.0.

About Privacy Terms Contact

© 2026 vitalwiki. Public-data based medicine & disease information.