ODCs

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1 OMIM reference -
1 associated gene
1 sign/symptom

PROTEIN INTERACTIONS: 1

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

Supravalvular aortic stenosis

Autosomal dominant severe congenital neutropenia

ELN	(UniProt - OMIM)		ELANE	(UniProt - OMIM)
			GFI1	(UniProt - OMIM)


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

Citations in the biomedical literature:

Supravalvular aortic stenosis		Autosomal dominant severe congenital neutropenia
	Synonym(s): - SVAS - Supravalvar aortic stenosis		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare surgical cardiac disease		Classification (Orphanet): - Rare genetic disease - Rare immune disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: variable Average age of death: no data available Type of inheritance: autosomal dominant		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: 1 OMIM reference - 1 MeSH reference: D021921		External references: 4 OMIM references - No MeSH references

Supravalvular aortic stenosis
	Very frequent - Cardiac rhythm disorder / arrhythmia
Autosomal dominant severe congenital neutropenia
(no data available)