EFO_0022607 (sulfate transporter-related osteochondrodysplasia) can be described as follows. Sulfate transporter-related osteochondrodysplasias are a group of inherited diseases caused by mutations in a gene called SLC26A2, which plays a role in cartilage and bone formation. These diseases include achondrogenesis type Ib, diastrophic dysplasia, atelosteogenesis type II, and recessive multiple epiphyseal dysplasia. Also known as: DTDST-related dysplasias.