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Hyper-IgM syndrome type 4

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ORPHA:101091

Classification level: Subtype of disorder

Synonym(s):
  • HIGM4

Prevalence: -

Inheritance: -

Age of onset:

ICD-10: D80.5

ICD-11: 4A01.1Y

OMIM: 608184

UMLS: C1842413

MeSH: C564277

GARD: 10580

Summary

This disease is described under Hyper-IgM syndrome without susceptibility to opportunistic infections

Detailed information

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

General public
Article for general public
Français (2007.pdf) - IPOPI
Deutsch (2007.pdf) - IPOPI
Ελληνικά (2007.pdf) - IPOPI
English (2007.pdf) - IPOPI
Eesti (2007.pdf) - IPOPI
Español (2007.pdf) - IPOPI
Русский (2007.pdf) - IPOPI
Română (2007.pdf) - IPOPI
العربية (2007.pdf) - IPOPI
Português (2007.pdf) - IPOPI
Guidelines
Emergency guidelines
Français (2020.pdf) - Orphanet Urgences
Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Newborn screening

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