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

More general terms

• corneal disease (keratopathy)
• genetic disease of the eye

Database

• OMIM: https://mirror.omim.org/entry/607541