Deafness - optic atrophy syndrome (Q55786): Difference between revisions

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Atrofia óptica autossômica dominante e surdez congênita é uma forma de atrofia óptica autossômica dominante, caracterizada por surdez severa congênita e insuficiência visual progressiva na meia-idade.
description / endescription / en
 
Autosomal dominant optic atrophy and congenital deafness is a form of autosomal dominant optic atrophy, characterised by congenital severe deafness and progressive mid-life visual failure.
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Property / Canonical URI: https://id.who.int/icd/entity/412176667 / rank
 
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CID11:ID_412176667
Property / CURIE: CID11:ID_412176667 / rank
 
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dki-india-ID_412176667
Property / Canary Token: dki-india-ID_412176667 / rank
 
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Concluído
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
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CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 03:27, 14 August 2026

Autosomal dominant optic atrophy and congenital deafness is a form of autosomal dominant optic atrophy, characterised by congenital severe deafness and progressive mid-life visual failure.
Language Label Description Also known as
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ID_412176667
    English
    Deafness - optic atrophy syndrome
    Autosomal dominant optic atrophy and congenital deafness is a form of autosomal dominant optic atrophy, characterised by congenital severe deafness and progressive mid-life visual failure.

      Statements

      CID11:ID_412176667
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      dki-india-ID_412176667
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      Concluído
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      13 August 2026
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