ODCs

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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

Recurrent infection due to specific granule deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CEBPA	(0.8)	CEBPE

Citations in the biomedical literature:

Acute myeloid leukemia with CEBPA somatic mutations		Recurrent infection due to specific granule deficiency
	Synonym(s): - AML with CEBPA somatic mutations		Synonym(s): - Neutrophil-specific granule deficiency

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease - Rare immune disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: - Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.