ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Acute myeloid leukemia with CEBPA somatic mutations

Acute necrotizing encephalopathy of childhood

CEBPA	(UniProt - OMIM)		CPT2	(UniProt - OMIM)
			RANBP2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CEBPA	(0.63)	RANBP2

Citations in the biomedical literature:

Acute myeloid leukemia with CEBPA somatic mutations		Acute necrotizing encephalopathy of childhood
	Synonym(s): - AML with CEBPA somatic mutations		Synonym(s): - ANEC - Isolated ANE - Isolated acute necrotizing encephalopathy

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare infectious disease - Rare neurologic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: sporadic

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

No signs/symptoms info available.