ODCs

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1 OMIM reference -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Ewing sarcoma

Xeroderma pigmentosum complementation group G


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EWSR1	(0.63)	ERCC5

Citations in the biomedical literature:

Ewing sarcoma		Xeroderma pigmentosum complementation group G
	Synonym(s): (no synonyms)		Synonym(s): - XPG

	Classification (Orphanet): - Rare bone disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare oncologic disease - Rare otorhinolaryngologic disease - Rare skin disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: sporadic		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.