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4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Extraskeletal Ewing sarcoma
Spinocerebellar ataxia type 19/22

ERG KCND3
EWSR1
FLI1
SMARCA5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EWSR1
(0.63)
KCND3



Citations in the biomedical literature:


Extraskeletal Ewing sarcoma
ERG EWSR1 FLI1 SMARCA5
Spinocerebellar ataxia type 19/22
KCND3



Extraskeletal Ewing sarcoma
Spinocerebellar ataxia type 19/22

Synonym(s):
- EOE
- Extraosseous Ewing sarcoma
- Extraosseous Ewing tumor
- Extraskeletal Ewing tumor

Synonym(s):
- SCA19/22

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C537198

No signs/symptoms info available.