ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Autosomal dominant keratitis

Familial retinoblastoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PAX6	(0.75)	RB1

Citations in the biomedical literature:

Autosomal dominant keratitis		Familial retinoblastoma
	Synonym(s): - Hereditary keratitis		Synonym(s): - Bilateral retinoblastoma - Hereditary retinoblastoma

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

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: normal 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: 1 OMIM reference - 1 MeSH reference: C537022		External references: No OMIM references No MeSH references

No signs/symptoms info available.