Catalog

Brachyolmia type 3

No MMS code

Link to WHO Definition

Brachyolmia type 3 – http://id.who.int/icd/entity/589025803

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.