Monarch Disease Ontology term MONDO_0013067 (cataract 34 multiple types) is any cataract (disease) in which the cause of the disease is a mutation in the FOXE3 gene. Also known as: CATC3, CTRCT34, FOXE3 cataract (disease), autosomal recessive congenital cataract 3, cataract (disease) caused by mutation in FOXE3, cataract 34 multiple types with or without microcornea.