Orphanet: Hyper IgM syndrome type 2

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Hyper-IgM syndrome type 2

ORPHA:101089

Classification level: Subtype of disorder

Synonym(s):
- AID deficiency
- Activation-induced cytidine deaminase deficiency
- HIGM2
Prevalence: -
Inheritance: -
Age of onset: -
ICD-10: D80.5
ICD-11: 4A01.05
OMIM: 605258
UMLS: C1720956
MeSH: -
GARD: 10578
MedDRA: -

Summary

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

Detailed information

General public

Article for general public
Arabic (2007, pdf) - IPOPI
Deutsch (2007, pdf) - IPOPI
Greek (2007, pdf) - IPOPI
English (2007, pdf) - IPOPI
Español (2007, pdf) - IPOPI
Eesti keel (2007, pdf) - IPOPI
Français (2007, pdf) - IPOPI
Português (2007, pdf) - IPOPI
Romanian (2007, pdf) - IPOPI
Russian (2007, pdf) - IPOPI

produced/endorsed by ERN(s) FSMR

produced/endorsed by FSMR(s)

Additional information

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Eurordis directory

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