Autosomal dominant brachyolmia

MONDO:0007232

Autosomal 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.

Also known as: brachyolmia type 3, brachyolmia, autosomal dominant, BCYM3, brachyolmia autosomal dominant, brachyrachia

35 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by