Cytoscape Web
Click node...


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

EIF2B1 APP
EIF2B2 PSEN1
EIF2B3 PSEN2
EIF2B4 SORL1
EIF2B5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EIF2B2
EIF2B5
(0.56)
(0.56)
APP
APP



Citations in the biomedical literature:


Ovarioleukodystrophy
EIF2B1 EIF2B2 EIF2B3 EIF2B4 EIF2B5
Early-onset autosomal dominant Alzheimer disease
APP PSEN1 PSEN2 SORL1



Ovarioleukodystrophy
Early-onset autosomal dominant Alzheimer disease

Synonym(s):
(no synonyms)

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

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic 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:
(no data available)
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:
1 OMIM reference -
No MeSH references
External references:
16 OMIM references -
No MeSH references

No signs/symptoms info available.