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1 OMIM reference -
5 associated genes
No signs/symptoms info
COMMON GENES: 5
PROTEIN INTERACTIONS: 9
1 OMIM reference -
5 associated genes
No signs/symptoms info
Ovarioleukodystrophy
Cree leukoencephalopathy

EIF2B1 EIF2B1
EIF2B2 EIF2B2
EIF2B3 EIF2B3
EIF2B4 EIF2B4
EIF2B5 EIF2B5


COMMON
GENES
EIF2B1
EIF2B2
EIF2B3
EIF2B4
EIF2B5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EIF2B1
EIF2B3
EIF2B4
EIF2B2
EIF2B1
EIF2B1
EIF2B2
EIF2B2
EIF2B3
(0.97)
(0.93)
(0.93)
(0.92)
(0.83)
(0.83)
(0.75)
(0.74)
(0.59)
EIF2B5
EIF2B5
EIF2B5
EIF2B5
EIF2B2
EIF2B3
EIF2B4
EIF2B3
EIF2B4



Citations in the biomedical literature:


Ovarioleukodystrophy
EIF2B1 EIF2B2 EIF2B3 EIF2B4 EIF2B5
Cree leukoencephalopathy



Ovarioleukodystrophy
Cree leukoencephalopathy

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):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

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

No signs/symptoms info available.