ODCs

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

PROTEIN INTERACTIONS: 2

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

Osteogenesis imperfecta type 2

Congenital stromal corneal dystrophy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COL1A2 COL1A1	(0.66) (0.63)	DCN DCN

Citations in the biomedical literature:

Osteogenesis imperfecta type 2		Congenital stromal corneal dystrophy
	Synonym(s): - Lethal osteogenesis imperfecta - OI type 2		Synonym(s): - CSCD - Congenital hereditary stromal dystrophy - Witschel dystrophy

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the eye and adnexa -

	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: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.