ODCs

Click node...

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

PROTEIN INTERACTIONS: 2

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

Microcystic corneal dystrophy

Osteogenesis imperfecta type 2


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TGFBI TGFBI	(0.63) (0.62)	COL1A1 COL1A2

Citations in the biomedical literature:

Microcystic corneal dystrophy		Osteogenesis imperfecta type 2
	Synonym(s): (no synonyms)		Synonym(s): - Lethal osteogenesis imperfecta - OI type 2

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

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

	Epidemiological data: (no data available)		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

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

No signs/symptoms info available.