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Congenital cataract microcornea with corneal opacity
2 associated genes
2 connected diseases
No signs/symptoms info
Disease Type of connection
Congenital blindness due to retinal non-attachment
Persistent hyperplastic primary vitreous
Synonym(s):
- CCMCO
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
ATOH7 Q8N100609875
PXDN Q92626605158
No signs/symptoms info available.