MONDO_0010111 (odontotrichomelic syndrome) is characterized by malformations of all four extremities, hypoplastic nails, ear anomalies, hypotrichosis, abnormal dentition, hyperhidrosis and nasolacrimal duct obstruction. So far, it has been described in less than 10 patients. Transmission is autosomal recessive. Also known as: Freire-Maia odontotrichomelic syndrome, Freire-Maia syndrome, odontotrichomelic hypohidrotic dysplasia, tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities.