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1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 3
3 associated genes
No signs/symptoms info
Spinocerebellar ataxia type 26
Dedifferentiated liposarcoma

EEF2 CDK4
SCA26 HMGA2
MDM2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EEF2
SCA26
SCA26
(0.63)
(0.63)
(0.63)
MDM2
CDK4
MDM2



Citations in the biomedical literature:


Spinocerebellar ataxia type 26
EEF2 SCA26
Dedifferentiated liposarcoma
CDK4 HMGA2 MDM2



Spinocerebellar ataxia type 26
Dedifferentiated liposarcoma

Synonym(s):
- SCA26

Synonym(s):
- DDLS

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -

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

External references:
1 OMIM reference -
1 MeSH reference: C537203
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.