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

ALB
(UniProt - OMIM)
 IGHG2
(UniProt - OMIM)
IGKC
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ALB
ALB
(0.72)
(0.72)
IGHG2
IGKC


Citations in the biomedical literature:


Congenital analbuminemia
ALB
Recurrent infections associated with rare immunoglobulin isotypes deficiency
IGHG2 IGKC



Congenital analbuminemia
Recurrent infections associated with rare immunoglobulin isotypes deficiency

Synonym(s):
(no synonyms)

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 hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: unknown
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.