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Hyper-IgM syndrome type 4

ORPHA101091
Synonym(s) HIGM4
Prevalence -
Inheritance -
Age of onset -
ICD-10
  • D80.5
OMIM
UMLS -
MeSH -
MedDRA -

Summary

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


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