ODCs

Click node...

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

Granular corneal dystrophy type II


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

Citations in the biomedical literature:

Osteogenesis imperfecta type 2		Granular corneal dystrophy type II
	Synonym(s): - Lethal osteogenesis imperfecta - OI type 2		Synonym(s): - Avellino corneal dystrophy - GCD2 - GCDII - Granular corneal dystrophy type 2 - Granular-lattice corneal 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: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C535474

No signs/symptoms info available.