Cytoscape Web
Click node...


6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
5 associated genes
No signs/symptoms info
Semantic dementia
Ovarioleukodystrophy

C9ORF72 EIF2B1
CHMP2B EIF2B2
GRN EIF2B3
MAPT EIF2B4
PSEN1 EIF2B5
VCP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
C9ORF72
(0.63)
EIF2B2



Citations in the biomedical literature:


Semantic dementia
C9ORF72 CHMP2B GRN MAPT PSEN1 VCP

Ovarioleukodystrophy
EIF2B1 EIF2B2 EIF2B3 EIF2B4 EIF2B5



Semantic dementia
Ovarioleukodystrophy

Synonym(s):
- Semantic primary progressive aphasia
- Semantic variant PPA

Synonym(s):
(no synonyms)

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

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

Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.