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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Lipoprotein glomerulopathy
Familial renal amyloidosis due to Apolipoprotein AII variant

APOE APOA2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APOE
(0.49)
APOA2



Citations in the biomedical literature:


Lipoprotein glomerulopathy
APOE
Familial renal amyloidosis due to Apolipoprotein AII variant
APOA2



Lipoprotein glomerulopathy
Familial renal amyloidosis due to Apolipoprotein AII variant

Synonym(s):
- LPG

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):
- Inborn errors of metabolism
- Rare endocrine disease
- 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:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
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.