Oral-facial-digital syndrome, type 10 is characterized by facial (telecanthus, flat nasal bridge, retrognathia), oral (cleft palate, vestibular frenula) and digital (oligodactyly, preaxial polydactyly) features, associated with remarkable radial shortening, fibular agenesis and coalescence of tarsal bones. The syndrome has been described in one 10-month-old girl. No new cases have been described since 1993. The disease is Monarch Disease Ontology term MONDO_0008137 (orofaciodigital syndrome X). Also known as: Figuera syndrome, OFD10, oral-facial-digital syndrome type 10, orofaciodigital syndrome type 10, orofaciodigital syndrome type X, orofaciodigital syndrome with fibular aplasia.