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ICD10 code of Aniridia and ICD9 code

What is the ICD10 code for Aniridia? And the ICD9 code for Aniridia?

ICD9 and ICD10 codes of Aniridia

The ICD-10 code for Aniridia is Q13.1, which is a congenital disorder characterized by the partial or complete absence of the iris. In the previous ICD-9 coding system, Aniridia was identified by the code 743.46. Aniridia can lead to various visual impairments and is often associated with other ocular abnormalities.
Aniridia is a rare genetic disorder characterized by the partial or complete absence of the iris, the colored part of the eye. The International Classification of Diseases (ICD) provides codes to classify medical conditions for various purposes, including billing and research.

The ICD-10 code for aniridia is Q13.1. This code falls under the category of "Congenital malformations of eye, ear, face, and neck." The specific code Q13.1 denotes "Aniridia." ICD-10 codes are alphanumeric codes used worldwide for consistent and standardized reporting of medical conditions.

On the other hand, the ICD-9 code for aniridia is 743.46. ICD-9 codes were widely used before the implementation of ICD-10. The code 743.46 represents "Aniridia," similar to the ICD-10 code.

These codes play a crucial role in medical documentation, as they help healthcare providers accurately identify and classify various conditions. They also facilitate data analysis, research, and communication between healthcare professionals.

It's important to note that the information provided here is for educational purposes only and should not replace professional medical advice. If you or someone you know is affected by aniridia, it is recommended to consult a healthcare professional for an accurate diagnosis and appropriate management.
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Stories of Aniridia

ANIRIDIA STORIES
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Sasha has Wagr syndrom: Aniridia, Willms tumor, mental dilays.
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My daughter is called abbie she is 9 years old she has aniridia and nystagmus . My daughter is not any different to any child her age apart limited vision she can do almost everything .when she got diagnosed at 6 week old I was deverstated thinking o...
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Born in rural Canada from a long family history of this disease, I am the 8th generation. My mom and grandfather have it and now my daughter also has it.  My Vision is about 20/100 and has remained stable throughout my young adult life up until no...
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My Daughter is almost 4 years old and has WAGR Syndrome, she was diagnosed with a wilms tumour when she was 14 months old and has had a year of chemotherapy and a full left nephrectomy. She wears transition prescription lenses and has done since she ...
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My daughter is 8 and was diagnosed with aniridia and nystagmus at 3 months old ❤️

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