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Autosomal dominant brachyolmia
rareAutosomal dominant brachyolmia is a relatively severe form of brachyolmia, a group of rare genetic skeletal disorders, characterized by short-trunked short stature, platyspondyly and kyphoscoliosis. Degenerative joint disease (osteoarthropathy) in the spine, large joints and interphalangeal joints becomes manifest in adulthood.
- Identifiers
- MONDO:0007232 OMIM:113500Orphanet:93304
- Causal genes
- TRPV4
- Also known as
- BCYM3 · brachyolmia autosomal dominant · brachyolmia type 3 · brachyolmia, autosomal dominant
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