ODCs

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

COMMON GENES: 1

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

Fuchs endothelial corneal dystrophy

Congenital hereditary endothelial dystrophy type II

Citations in the biomedical literature:

Fuchs endothelial corneal dystrophy		Congenital hereditary endothelial dystrophy type II
	Synonym(s): - Endoepithelial corneal dystrophy - FECD - Late hereditary endothelial dystrophy		Synonym(s): - Autosomal recessive CHED - Autosomal recessive congenital hereditary endothelial dystrophy - CHED2 - CHEDII - Congenital hereditary endothelial dystrophy type 2 - Infantile hereditary endothelial dystrophy - Maumenee corneal dystrophy

	Classification (Orphanet): - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): - Diseases of the eye and adnexa -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood 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 recessive

	External references: 8 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.