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

Cerebellar ataxia-deafness-narcolepsy syndrome

Unilateral retinoblastoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DNMT1	(0.88)	RB1

Citations in the biomedical literature:

Cerebellar ataxia-deafness-narcolepsy syndrome		Unilateral retinoblastoma
	Synonym(s): - ADCA-DN - Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		Synonym(s): - Non-familial retinoblastoma - Non-hereditary retinoblastoma

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood 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: sporadic

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

No signs/symptoms info available.