Search
Avellino corneal dystrophy
Genetics:
- autosomal dominant
- associated with defects in TGFBI
Differential diagnosis:
- may be a variant of corneal dystrophy granular type, with a significant amyloidogenic tendency
General
corneal disease (keratopathy)
genetic disease of the eye
Database Correlations
OMIM 607541
References
OMIM :accession 607541