Related MeSH Hierarchy (5)
Diseases [C] » Eye Diseases [C11] » Eye Abnormalities » Aniridia
Diseases [C] » Eye Diseases [C11] » Eye Diseases, Hereditary » Aniridia
Diseases [C] » Eye Diseases [C11] » Uveal Diseases » Iris Diseases » Aniridia
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Eye Abnormalities » Aniridia
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Eye Diseases, Hereditary » Aniridia
Description
A congenital abnormality in which there is only a rudimentary iris. This is due to the failure of the optic cup to grow. Aniridia also occurs in a hereditary form, usually autosomal dominant. MeSH
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Subtype Terms (1)
Phase 2 Indicated Drugs (1)
Organization Involved with Phase 2 Indications (1)
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