" /> Optic atrophy - CISMeF





ICD-11 code : 9C40.B;

Preferred Label : Optic atrophy;

ICD-11 definition : 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.;

ICD-11 synonym : second cranial nerve atrophy; second cranium nerve atrophy; OA - [optic atrophy]; Primary optic atrophy; optic nerve atrophy;

ICD-11 acronym : OA;

ICD-11 "unspecified" category code : 9C40.BZ;

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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.

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17/05/2024


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