aniridia
C2CEFR level
97/100Rarity: very rare
TechnicalRegister
A congenital, usually bilateral absence or severe hypoplasia of the iris.
The child's aniridia was associated with foveal hypoplasia and a mutation affecting the PAX6 gene.
Rarity runs from 0 (a word everyone knows) to 100 (almost never seen outside specialist or literary writing). Level is the word's real difficulty on the CEFR scale, from A1 to C2.
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