Cataract-aberrant oral frenula-growth delay syndrome is characterized by cataracts and short stature associated with variable anomalies, including aberrant oral frenula, a characteristic facial appearance (posteriorly angulated ears, upslanting palpebral fissures, small nose, ptosis and epicanthal folds) cavernous hemangiomas and hernias. It has been described in a mother and her two children. It is transmitted as an autosomal dominant trait. The disease is cataract-aberrant oral frenula-growth delay syndrome (Monarch Disease Ontology term MONDO_0007277). Also known as: Wellesley-Carman-French syndrome.