ODCs

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

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Osteogenesis imperfecta type 2

Ehlers-Danlos syndrome, vascular-like type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COL1A2	(0.62)	COL1A1

Citations in the biomedical literature:

Osteogenesis imperfecta type 2		Ehlers-Danlos syndrome, vascular-like type
	Synonym(s): - Lethal osteogenesis imperfecta - OI type 2		Synonym(s): - EDS, vascular-like type

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease		Classification (Orphanet): - Rare circulatory system disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare skin disease - Rare systemic or rheumatologic 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: before age 5 Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 4 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.