obsolete_Axenfeld-Rieger syndrome true MedDRA:10059255 UMLS:C0265341 orphanet Axenfeld-Rieger syndrome (ARS) is a generic term used to designate overlapping genetic disorders, in which the major physical condition is anterior segment dysgenesis of the eye. Patients with ARS may also present with multiple variable congenital anomalies. OMIM:601499 http://purl.obolibrary.org/obo/MONDO_0019187 OMIM:180500 Replaced with Mondo term. 3.41.0 Rieger syndrome MESH:C535679 Axenfeld syndrome ICD10:Q13.8 OMIM:602482