Deafness – onychodystrophy, autosomal dominant (Q98483): Difference between revisions

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Property / Canonical URI: https://id.who.int/icd/entity/1712445563 / rank
 
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CID11:ID_1712445563
Property / CURIE: CID11:ID_1712445563 / rank
 
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dki-india-ID_1712445563
Property / Canary Token: dki-india-ID_1712445563 / rank
 
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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15 August 2026
Timestamp+2026-08-15T00:00:00Z
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Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 14:59, 16 August 2026

Autosomal dominant deafness-onychodystrophy syndrome is a very rare condition characterised by congenital hearing impairment, absent or hypoplastic nails on the hands and feet and brachydactyly.
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ID_1712445563
    English
    Deafness – onychodystrophy, autosomal dominant
    Autosomal dominant deafness-onychodystrophy syndrome is a very rare condition characterised by congenital hearing impairment, absent or hypoplastic nails on the hands and feet and brachydactyly.

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      CID11:ID_1712445563
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      dki-india-ID_1712445563
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      Concluído
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      15 August 2026
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