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Synpolydactyly type 2

1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Supravalvular aortic stenosis

1 OMIM reference -
1 associated gene
1 sign/symptom

Synpolydactyly type 2

Supravalvular aortic stenosis

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FBLN1	(0.85)	ELN

Citations in the biomedical literature:

Synpolydactyly type 2		Supravalvular aortic stenosis
	Synonym(s): - SD2, Debeer type - SD2b - SPD, Debeer type - SPD2 - Synpolydactyly, Debeer type		Synonym(s): - SVAS - Supravalvar aortic stenosis

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		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

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D021921

Supravalvular aortic stenosis
	Very frequent - Cardiac rhythm disorder / arrhythmia
Synpolydactyly type 2
(no data available)