Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing lossAxenfeld-Rieger syndrome caused by mutation in FOXC1Axenfeld-Rieger syndrome type 3FOXC1 Axenfeld-Rieger syndromeRIEG3Rieger syndrome type 3anterior chamber cleavage syndromeAxenfeld anomalyAxenfeld-Rieger anomalyAxenfeld-Rieger anomaly with Cardiac defects and/Or sensorineural hearing lossAxenfeld-Rieger anomaly with or without Cardiac defects and/or sensorineural hearing lossAxenfeld-Rieger syndrome, type 3Rieger anomalyRieger syndrome, type 3anterior chamber Cleavage syndromeanterior segment mesenchymal dysgenesis
Definition
Any Axenfeld-Rieger syndrome in which the cause of the disease is a mutation in the FOXC1 gene.
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