Axenfeld-Rieger syndrome type 3

Any Axenfeld-Rieger syndrome in which the cause of the disease is a mutation in the FOXC1 gene.

Also known as: Axenfeld-Rieger syndrome caused by mutation in FOXC1, Axenfeld-Rieger syndrome type 3, FOXC1 Axenfeld-Rieger syndrome, RIEG3, anterior chamber cleavage syndrome, Axenfeld anomaly, Axenfeld-Rieger anomaly, Axenfeld-Rieger anomaly with Cardiac defects and/Or sensorineural hearing loss

15 clinical trials for this condition and its sub-types.