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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
Isolated adermatoglyphia

ERG SMARCAD1
EWSR1
FLI1
SMARCA5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SMARCA5
(0.63)
SMARCAD1



Citations in the biomedical literature:


Extraskeletal Ewing sarcoma
ERG EWSR1 FLI1 SMARCA5
Isolated adermatoglyphia
SMARCAD1



Extraskeletal Ewing sarcoma
Isolated adermatoglyphia

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

Synonym(s):
- Absence of fingerprints
- Immigration delay disease

Classification (Orphanet):
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.