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1 OMIM reference -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
4 associated genes
No signs/symptoms info
Cree leukoencephalopathy
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis

EIF2B1 ARHGDIA
EIF2B2 PLCE1
EIF2B3 PTPRO
EIF2B4 WT1
EIF2B5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EIF2B1
(0.76)
ARHGDIA



Citations in the biomedical literature:


Cree leukoencephalopathy
EIF2B1 EIF2B2 EIF2B3 EIF2B4 EIF2B5
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
ARHGDIA PLCE1 PTPRO WT1



Cree leukoencephalopathy
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis

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

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

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

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

No signs/symptoms info available.