Congenital aphakia (Q46081): Difference between revisions
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13 August 2026
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| Property / Linked ICD 10: Q12.3 / rank | |||||||||||||||
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Latest revision as of 14:25, 13 August 2026
Congenital primary aphakia is a developmental eye defect characterised by an absence of the lens, and can be associated with variable secondary ocular defects (including aplasia/dysplasia of the anterior segment of the eye, microphthalmia, and in some cases absence of the iris, retinal dysplasia, or sclerocornea).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LA12.2 |
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| English | Congenital aphakia |
Congenital primary aphakia is a developmental eye defect characterised by an absence of the lens, and can be associated with variable secondary ocular defects (including aplasia/dysplasia of the anterior segment of the eye, microphthalmia, and in some cases absence of the iris, retinal dysplasia, or sclerocornea). |
Statements
CID11:LA12.2
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dki-india-LA12.2
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Concluído
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13 August 2026
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