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

Rubinstein-Taybi syndrome due to 16p13.3 microdeletion


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RUNX1 CEBPA	(0.82) (0.52)	CREBBP CREBBP

Citations in the biomedical literature:

Acute myeloid leukemia with t(8;21)(q22;q22) translocation		Rubinstein-Taybi syndrome due to 16p13.3 microdeletion

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare oncologic disease - Rare renal disease

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

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

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

No signs/symptoms info available.