Björnstad syndrome (Q87746): Difference between revisions
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Revision as of 13:39, 15 August 2026
Björnstad syndrome is a genetic syndrome characterised by congenital sensorineural hearing loss and pili torti.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2035502746 |
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| English | Björnstad syndrome |
Björnstad syndrome is a genetic syndrome characterised by congenital sensorineural hearing loss and pili torti. |
Statements
CID11:ID_2035502746
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dki-india-ID_2035502746
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