Short Stature, Amelogenesis imperfecta, and Skeletal dysplasia with Scoliosis (SSASKS, OMIM #618,363) was first related to mutations in the solute carrier family 10 member 7 (SLC10A7) gene (OMIM #611,459) in 2018 [1]. The gene discussed is SLC10A7; the disease is skeletal dysplasia.