Optic atrophy (Q41885): Difference between revisions

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+https://id.who.int/icd/entity/568505454
@@ Property / Canonical URI: https://id.who.int/icd/entity/568505454 / rank @@
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@@ Property / CURIE @@
+CID11:9C40.B
@@ Property / CURIE: CID11:9C40.B / rank @@
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+Concluído
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+https://pauloleads.com.br/cases-publicos/
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+August 2026Timestamp +2026-08-13T00:00:00Z
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Calendar Gregorian
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@@ Property / Collection date: 13 August 2026 / rank @@
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+H46-H48
@@ Property / Linked ICD 10: H46-H48 / rank @@
+Normal rank

Latest revision as of 08:12, 13 August 2026

Optic atrophies (OA) refer to a specific group of hereditary optic neuropathies in which the cause of the optic nerve dysfunction is inherited either in an autosomal dominant or autosomal recessive pattern. Autosomal dominant optic atrophy (ADOA), type Kjer, is the most common OA, whereas autosomal recessive optic atrophy (AROA) is a rare form.

Language	Label	Description	Also known as
default for all languages	9C40.B
English	Optic atrophy	Optic atrophies (OA) refer to a specific group of hereditary optic neuropathies in which the cause of the optic nerve dysfunction is inherited either in an autosomal dominant or autosomal recessive pattern. Autosomal dominant optic atrophy (ADOA), type Kjer, is the most common OA, whereas autosomal recessive optic atrophy (AROA) is a rare form.