Oculodental syndrome, Rutherfurd type is a rare genetic disorder that is primarily characterized by the classical triad of gingival fibromatosis, non-eruption of tooth and corneal dystrophy (bilateral corneal vascularization and opacity). Abnormally shaped teeth have also been reported. The syndrome is transmitted as an autosomal dominant trait. The disease is oculodental syndrome, Rutherfurd type (MONDO_0008396, a Monarch Disease Ontology id). Also known as: Rutherfurd syndrome, corneal dystrophy with gum Hypertrophy, corneal dystrophy with gum hypertrophy, gingival Hypertrophy with corneal dystrophy, gingival hypertrophy corneal dystrophy, gingival hypertrophy-corneal dystrophy.