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Congenital analbuminemia
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial renal amyloidosis due to Apolipoprotein AII variant
1 associated gene
No signs/symptoms info
Congenital analbuminemia
Familial renal amyloidosis due to Apolipoprotein AII variant

ALB
(UniProt - OMIM)
 APOA2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ALB
(0.72)
APOA2


Citations in the biomedical literature:


Congenital analbuminemia
ALB
Familial renal amyloidosis due to Apolipoprotein AII variant
APOA2



Congenital analbuminemia
Familial renal amyloidosis due to Apolipoprotein AII variant

Synonym(s):
(no synonyms)

Synonym(s):
- Apolipoprotein AII amyloidosis
- Familial amyloid nephropathy due to apolipoprotein AII variant
- Hereditary amyloid nephropathy due to Apolipoprotein AII variant
- Hereditary renal amyloidosis due to apolipoprotein AII variant
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
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:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.