ODCs

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

PROTEIN INTERACTIONS: 1

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

Cerebellar ataxia-deafness-narcolepsy syndrome

Familial platelet syndrome with predisposition to acute myelogenous leukemia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DNMT1	(0.73)	RUNX1

Citations in the biomedical literature:

Cerebellar ataxia-deafness-narcolepsy syndrome		Familial platelet syndrome with predisposition to acute myelogenous leukemia
	Synonym(s): - ADCA-DN - Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome		Synonym(s): - FPD/AML syndrome - FPS/AML syndrome - Familial platelet disorder with associated myeloid malignancy - Familial platelet syndrome

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	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: <1 / 1 000 000 Average age onset: no data available Average age of death: no data available Type of inheritance: autosomal dominant

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

No signs/symptoms info available.