ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Anaplastic ependymoma

Autosomal dominant severe congenital neutropenia

C11ORF95	(UniProt - OMIM)		ELANE	(UniProt - OMIM)
RELA	(UniProt - OMIM)		GFI1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RELA	(0.73)	GFI1

Citations in the biomedical literature:

Anaplastic ependymoma		Autosomal dominant severe congenital neutropenia
	Synonym(s): - High-grade ependymoma		Synonym(s): (no synonyms)

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

	Classification (ICD10): (no data available)		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 No MeSH references		External references: 4 OMIM references - No MeSH references

No signs/symptoms info available.