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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
Familial renal amyloidosis due to Apolipoprotein AI variant
1 associated gene
No signs/symptoms info
Recurrent infections associated with rare immunoglobulin isotypes deficiency
Familial renal amyloidosis due to Apolipoprotein AI variant

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
Familial renal amyloidosis due to Apolipoprotein AI variant
APOA1



Recurrent infections associated with rare immunoglobulin isotypes deficiency
Familial renal amyloidosis due to Apolipoprotein AI variant

Synonym(s):
- IgG subclass deficiency with IgA subclass deficiency
- Isolated IgG subclass deficiency
- Kappa-chain deficiency
- Selective IgG subclass deficiency
Synonym(s):
- Apolipoprotein AI amyloidosis
- Familial amyloid nephropathy due to apolipoprotein AI variant
- Hereditary amyloid nephropathy due to apolipoprotein AI variant
- Hereditary renal amyloidosis due to apolipoprotein AI variant
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal 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:
No OMIM references
No MeSH references
No signs/symptoms info available.