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gelatinous drop-like corneal dystrophy; lattice corneal dystrophy type 3
Genetics:
- autosomal recessive
- associated with defects in TACSTD2
Clinical manifestations:
- grayish corneal amyloid deposits that cause severe visual impairment
General
corneal disease (keratopathy)
genetic disease of the eye
Database Correlations
OMIM 204870
References
UniProt :accession P09758