Deafness – onychodystrophy, autosomal dominant (Q98483): Difference between revisions
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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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1712445563 |
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| 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. |
Statements
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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