Cytoscape Web
Click node...


2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
16 OMIM references -
4 associated genes
No signs/symptoms info
Hyperlipoproteinemia type 4
Early-onset autosomal dominant Alzheimer disease

APOA5 APP
LIPI PSEN1
PSEN2
SORL1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APOA5
(0.72)
SORL1



Citations in the biomedical literature:


Hyperlipoproteinemia type 4
APOA5 LIPI
Early-onset autosomal dominant Alzheimer disease
APP PSEN1 PSEN2 SORL1



Hyperlipoproteinemia type 4
Early-onset autosomal dominant Alzheimer disease

Synonym(s):
- Familial hypertriglyceridemia

Synonym(s):
- EOFAD
- Early-onset familial autosomal dominant Alzheimer disease
- Familial Alzheimer disease

Classification (Orphanet):
- Inborn errors of metabolism
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: no data available
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: autosomal dominant

External references:
2 OMIM references -
1 MeSH reference: D006953
External references:
16 OMIM references -
No MeSH references

No signs/symptoms info available.