Spondylocarpotarsal synostosis syndrome is associated with both autosomal dominant and recessive inheritance; both missense and nonsense MYH3 variants have been reported in recessive cases (Carapito et al, 2016; Zieba et al, 2017; Cameron‐Christie et al, 2018). The gene discussed is MYH3; the disease is Spondylocarpotarsal synostosis.