ODCs

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5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

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

Acute myeloid leukemia with t(8;21)(q22;q22) translocation

Cerebellar ataxia-deafness-narcolepsy syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RUNX1 RUNX1T1	(0.73) (0.73)	DNMT1 DNMT1

Citations in the biomedical literature:

Acute myeloid leukemia with t(8;21)(q22;q22) translocation		Cerebellar ataxia-deafness-narcolepsy syndrome
	Synonym(s): (no synonyms)		Synonym(s): - ADCA-DN - Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome

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

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.