Monarch Disease Ontology id 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.