Oculotrichodysplasia is characterized by retinitis pigmentosa, trichodysplasia, dental anomalies, and onychodysplasia. It has been described in two siblings (brother and sister) born to first cousin parents. Transmission appears to be autosomal recessive. The disease is Monarch Disease Ontology id MONDO_0009771 (oculotrichodysplasia). Also known as: Cecato de Lima-Pinheiro syndrome.