There are several other SHFM and oral cleft disorders, some of which include both, such as ectrodactyly, ectodermal dysplasia, cleft lip/palate syndrome‐1 (EEC1), and ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome‐3 (EEC3) which are autosomal dominant disorders that include SHFM as well as skin anomalies. This evidence concerns the gene TP63 and ectodermal dysplasia syndrome.