ODCs

Click node...

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Acute myeloid leukemia with CEBPA somatic mutations

Rubinstein-Taybi syndrome due to 16p13.3 microdeletion


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

Citations in the biomedical literature:

Acute myeloid leukemia with CEBPA somatic mutations		Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
	Synonym(s): - AML with CEBPA somatic mutations		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - 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.