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Recurrent infections associated with rare immunoglobulin isotypes deficiency
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Primary systemic amyloidosis
1 OMIM reference -
1 associated gene
No signs/symptoms info
Recurrent infections associated with rare immunoglobulin isotypes deficiency
Primary systemic amyloidosis

IGHG2
(UniProt - OMIM)
 APOA1
(UniProt - OMIM)
IGKC
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
IGKC
(0.72)
APOA1


Citations in the biomedical literature:


Recurrent infections associated with rare immunoglobulin isotypes deficiency
IGHG2 IGKC
Primary systemic amyloidosis
APOA1



Recurrent infections associated with rare immunoglobulin isotypes deficiency
Primary systemic amyloidosis

Synonym(s):
- IgG subclass deficiency with IgA subclass deficiency
- Isolated IgG subclass deficiency
- Kappa-chain deficiency
- Selective IgG subclass deficiency
Synonym(s):
- Systemic AL amyloidosis
- Systemic immunoglobulinic amyloidosis
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare hematologic disease
- Rare neurologic disease
- Rare oncologic disease
- Rare renal disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: unknown
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.