An Axenfeld-Rieger syndrome that has_material_basis_in heterozygous mutation in the FOXC1 gene on chromosome 6p25. [ http://purl.obolibrary.org/obo/ECO_0007645 url:https://www.ncbi.nlm.nih.gov/pubmed/9792859 ]
Synonyms: anterior segment mesenchymal dysgenesis Rieger syndrome type 3 anterior chamber cleavage syndrome Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss RIEG3