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1 OMIM reference -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
3 associated genes
No signs/symptoms info
Ovarioleukodystrophy
Frontotemporal dementia with motor neuron disease

EIF2B1 C9ORF72
EIF2B2 FUS
EIF2B3 TARDBP
EIF2B4
EIF2B5


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Ovarioleukodystrophy
EIF2B1 EIF2B2 EIF2B3 EIF2B4 EIF2B5
Frontotemporal dementia with motor neuron disease
C9ORF72 FUS TARDBP



Ovarioleukodystrophy
Frontotemporal dementia with motor neuron disease

Synonym(s):
(no synonyms)

Synonym(s):
- FTD-ALS
- FTD-MND
- Frontotemporal dementia with amyotrophic lateral sclerosis

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):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: adult
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.