Q13.1
ICD-10-CMThis code describes aniridia, a rare congenital ocular disorder characterized by the partial or complete absence of the iris, the colored part of the eye. This condition often affects both eyes and can lead to significant visual impairment due to associated ocular abnormalities.
Use this code when documentation clearly indicates a diagnosis of aniridia, whether congenital or acquired, though it is predominantly congenital. Supporting documentation will typically include ophthalmological examination findings detailing the absence or hypoplasia of the iris.
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