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Familial renal amyloidosis due to Apolipoprotein AII variant
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Idiopathic bronchiectasis
3 OMIM references -
4 associated genes
No signs/symptoms info
Familial renal amyloidosis due to Apolipoprotein AII variant
Idiopathic bronchiectasis

APOA2
(UniProt - OMIM)
 CFTR
(UniProt - OMIM)
SCNN1A
(UniProt - OMIM)
SCNN1B
(UniProt - OMIM)
SCNN1G
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
APOA2
(0.63)
CFTR


Citations in the biomedical literature:


Familial renal amyloidosis due to Apolipoprotein AII variant
APOA2
Idiopathic bronchiectasis
CFTR SCNN1A SCNN1B SCNN1G



Familial renal amyloidosis due to Apolipoprotein AII variant
Idiopathic bronchiectasis

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
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare respiratory disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the respiratory system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
No MeSH references
No signs/symptoms info available.