Orphanet: X linked hyper IgM syndrome
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X-linked hyper-IgM syndrome

ORPHA:101088

Classification level: Subtype of disorder
  • Synonym(s):
    • HIGM1
    • Hyper-IgM syndrome due to CD40 ligand deficiency
    • Hyper-IgM syndrome due to CD40L deficiency
    • Hyper-IgM syndrome type 1
    • XHIGM
  • Prevalence: -
  • Inheritance: X-linked recessive 
  • Age of onset: -
  • ICD-10: D80.5
  • OMIM: 308230
  • UMLS: C0398689
  • MeSH: -
  • GARD: 73
  • MedDRA: -

Summary

This disease is described under Hyper-IgM syndrome with susceptibility to opportunistic infections

  A summary on this disease is available in

Detailed information

General public

Disease review articles

ERN : produced/endorsed by ERN(s)
FSMR : produced/endorsed by FSMR(s)

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