ODCs

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

COMMON GENES: 1

2 associated genes
No signs/symptoms info

Congenital blindness due to retinal non-attachment

Congenital cataract microcornea with corneal opacity

ATOH7	(UniProt - OMIM)		ATOH7	(UniProt - OMIM)
			PXDN	(UniProt - OMIM)

Citations in the biomedical literature:

Congenital blindness due to retinal non-attachment		Congenital cataract microcornea with corneal opacity
	Synonym(s): - Congenital retinal detachment - NCRNA disease - Non-syndromic congenital retinal non-attachment		Synonym(s): - CCMCO

	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): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: no data available Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.