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congenital stromal corneal dystrophy (CSCD)
Pathology:
- bilateral, primary alterations of the cornea
- not associated with prior inflammation or secondary to systemic disease
Genetics:
- generally autosomal dominant
- associated with defects in decorin (DCN)
General
genetic disease of the eye
corneal disease (keratopathy)
Database Correlations
OMIM 610048
References
OMIM :accession 610048