Cytoscape Web
Click node...


1 OMIM reference -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
5 signs/symptoms
Ewing sarcoma
X-linked epilepsy - learning disabilities - behavior disorders

ERG SYN1
ETV1
ETV4
EWSR1
FLI1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ERG
(0.68)
SYN1



Citations in the biomedical literature:


Ewing sarcoma
ERG ETV1 ETV4 EWSR1 FLI1
X-linked epilepsy - learning disabilities - behavior disorders
SYN1



Ewing sarcoma
X-linked epilepsy - learning disabilities - behavior disorders

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

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: x-linked recessive

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

X-linked epilepsy - learning disabilities - behavior disorders

Very frequent
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Macrocephaly / macrocrania / megalocephaly / megacephaly
- Psychic / behavioural troubles
- Seizures / epilepsy / absences / spasms / status epilepticus
- X-linked recessive inheritance



Ewing sarcoma

(no data available)