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Familial renal amyloidosis due to Apolipoprotein AII variant
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hyperlipidemia type 3
1 associated gene
No signs/symptoms info
Familial renal amyloidosis due to Apolipoprotein AII variant
Hyperlipidemia type 3

APOA2
(UniProt - OMIM)
 APOE
(UniProt - OMIM)

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


Citations in the biomedical literature:


Familial renal amyloidosis due to Apolipoprotein AII variant
APOA2
Hyperlipidemia type 3
APOE



Familial renal amyloidosis due to Apolipoprotein AII variant
Hyperlipidemia type 3

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):
- Broad-betalipoproteinemia
- Dyslipidemia type 3
- Familial dysbetalipoproteinemia
- Familial hyperlipoproteinemia type 3
- HLP type 3
- Hyperlipoproteinemia type 3
- Remnant disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: variable
Average age of death: normal
Type of inheritance: multigenic/multifactorial
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
1 MeSH reference: D006952
No signs/symptoms info available.