ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

4 OMIM references -
2 associated genes
No signs/symptoms info

Atypical chronic myeloid leukemia

Autosomal dominant severe congenital neutropenia

CSF3R	(UniProt - OMIM)		ELANE	(UniProt - OMIM)
			GFI1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CSF3R	(0.52)	ELANE

Citations in the biomedical literature:

Atypical chronic myeloid leukemia		Autosomal dominant severe congenital neutropenia
	Synonym(s): - Subacute myeloid leukemia		Synonym(s): (no synonyms)

	Classification (Orphanet): - 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: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant

	External references: No OMIM references 1 MeSH reference: D054438		External references: 4 OMIM references - No MeSH references

No signs/symptoms info available.