Achondrogenesis is a rare genetic disorder that affects bone growth and development. Some synonyms for this condition include achondroplasia, chondrodysplasia, and spondyloepiphyseal dysplasia congenita. These conditions also affect bone growth and development, and can cause short stature, skeletal abnormalities, and joint problems. Achondrogenesis can be caused by mutations in several genes, including COL2A1, TRIP11, and SLC26A2. While there is no cure for achondrogenesis, treatments such as physical therapy, surgery, and medication can help manage the symptoms. Early intervention is important to ensure the best possible outcomes for individuals with this condition.