ODCs

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

PROTEIN INTERACTIONS: 1

Familial retinoblastoma

1 associated gene
No signs/symptoms info

Osteosarcoma

Familial retinoblastoma

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CHEK2	(0.79)	RB1

Citations in the biomedical literature:

Osteosarcoma		Familial retinoblastoma
	Synonym(s): - Osteogenic sarcoma		Synonym(s): - Bilateral retinoblastoma - Hereditary retinoblastoma

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

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Neoplasms -

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

	External references: 1 OMIM reference - 1 MeSH reference: D012516		External references: No OMIM references No MeSH references

No signs/symptoms info available.