Brachyolmia type 3 (Q101702): Difference between revisions
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Revision as of 18:32, 16 August 2026
Brachyolmia type 3 is an autosomal dominant, mildly severe form of brachyolmia, a group of rare genetic skeletal disorders, and is characterised by short stature, platyspondyly and severe kyphoscoliosis.
| Language | Label | Description | Also known as |
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| default for all languages | ID_589025803 |
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| English | Brachyolmia type 3 |
Brachyolmia type 3 is an autosomal dominant, mildly severe form of brachyolmia, a group of rare genetic skeletal disorders, and is characterised by short stature, platyspondyly and severe kyphoscoliosis. |
Statements
CID11:ID_589025803
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