ODCs

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

PROTEIN INTERACTIONS: 1

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

Granular corneal dystrophy type II

Hypochondrogenesis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TGFBI	(0.62)	COL2A1

Citations in the biomedical literature:

Granular corneal dystrophy type II		Hypochondrogenesis
	Synonym(s): - Avellino corneal dystrophy - GCD2 - GCDII - Granular corneal dystrophy type 2 - Granular-lattice corneal dystrophy		Synonym(s): (no synonyms)

	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: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.