Cytoscape Web
Click node...

Recurrent infections associated with rare immunoglobulin isotypes deficiency
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Juvenile glaucoma
6 OMIM references -
2 associated genes
No signs/symptoms info
Recurrent infections associated with rare immunoglobulin isotypes deficiency
Juvenile glaucoma

IGHG2
(UniProt - OMIM)
 CYP1B1
(UniProt - OMIM)
IGKC
(UniProt - OMIM)
 MYOC
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
IGKC
(0.63)
MYOC


Citations in the biomedical literature:


Recurrent infections associated with rare immunoglobulin isotypes deficiency
IGHG2 IGKC
Juvenile glaucoma
CYP1B1 MYOC



Recurrent infections associated with rare immunoglobulin isotypes deficiency
Juvenile glaucoma

Synonym(s):
- IgG subclass deficiency with IgA subclass deficiency
- Isolated IgG subclass deficiency
- Kappa-chain deficiency
- Selective IgG subclass deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: unknown
Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
6 OMIM references -
No MeSH references
No signs/symptoms info available.