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corneal endothelial dystrophy type 2; congenital hereditary endothelial dystrophy of cornea; Maumemee corneal dystrophy
Pathology:
- bilateral corneal dystrophy
Genetics:
- autosomal recessive
- associated with defects in SLC4A11
Clinical manifestations:
- corneal opacification
- nystagmus
General
corneal endothelial dystrophy; Chandler syndrome
Database Correlations
OMIM 217700
References
OMIM :accession 217700