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Osteogenesis imperfecta type 5

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

PROTEIN INTERACTIONS: 1

Supravalvular aortic stenosis

1 OMIM reference -
1 associated gene
1 sign/symptom

Osteogenesis imperfecta type 5

Supravalvular aortic stenosis

FKBP10	(UniProt - OMIM)		ELN	(UniProt - OMIM)
IFITM5	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FKBP10	(0.55)	ELN

Citations in the biomedical literature:

Osteogenesis imperfecta type 5		Supravalvular aortic stenosis
	Synonym(s): - OI type 5		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: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		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: 2 OMIM references - 1 MeSH reference: C536046		External references: 1 OMIM reference - 1 MeSH reference: D021921

Supravalvular aortic stenosis
	Very frequent - Cardiac rhythm disorder / arrhythmia
Osteogenesis imperfecta type 5
(no data available)