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X-linked hyper-IgM syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Recurrent infections associated with rare immunoglobulin isotypes deficiency
1 OMIM reference -
2 associated genes
No signs/symptoms info
X-linked hyper-IgM syndrome
Recurrent infections associated with rare immunoglobulin isotypes deficiency

CD40LG
(UniProt - OMIM)
 IGHG2
(UniProt - OMIM)
IGKC
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CD40LG
(0.52)
IGKC


Citations in the biomedical literature:


X-linked hyper-IgM syndrome
CD40LG
Recurrent infections associated with rare immunoglobulin isotypes deficiency
IGHG2 IGKC



X-linked hyper-IgM syndrome
Recurrent infections associated with rare immunoglobulin isotypes deficiency

Synonym(s):
- HIGM1
- Hyper-IgM syndrome due to CD40 ligand deficiency
- Hyper-IgM syndrome due to CD40L deficiency
- Hyper-IgM syndrome type 1
- XHIGM
Synonym(s):
- IgG subclass deficiency with IgA subclass deficiency
- Isolated IgG subclass deficiency
- Kappa-chain deficiency
- Selective IgG subclass deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: unknown
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.