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1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
C3 glomerulonephritis
Familial renal amyloidosis due to Apolipoprotein AI variant

CFHR1 APOA1
CFHR5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CFHR1
(0.62)
APOA1



Citations in the biomedical literature:


C3 glomerulonephritis
CFHR1 CFHR5
Familial renal amyloidosis due to Apolipoprotein AI variant
APOA1



C3 glomerulonephritis
Familial renal amyloidosis due to Apolipoprotein AI variant

Synonym(s):
(no synonyms)

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 renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
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.