ODCs

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3 OMIM references -
3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Neurofibromatosis type 3

Familial retinoblastoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SMARCB1	(0.52)	RB1

Citations in the biomedical literature:

Neurofibromatosis type 3		Familial retinoblastoma
	Synonym(s): - NF3 - Neurilemmomatosis - Schwannomatosis		Synonym(s): - Bilateral retinoblastoma - Hereditary retinoblastoma

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

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

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant

	External references: 3 OMIM references - 1 MeSH reference: C536641		External references: No OMIM references No MeSH references

No signs/symptoms info available.