syndromic disease hereditary disease iridogoniodysgenesis multiple congenital anomalies/dysmorphic syndrome without intellectual disability obsolete non-syndromic developmental defect of the eye obsolete syndromic anorectal malformation non-acquired combined pituitary hormone deficiency Axenfeld-Rieger syndrome https://github.com/monarch-initiative/mondo/issues/8786 https://rarediseases.info.nih.gov/diseases/5701/axenfeld-rieger-syndrome https://www.malacards.org/card/axenfeld_rieger_syndrome MEDGEN:501192 GARD:0005701 NCIT:C131001 ARS Rieger syndrome Axenfeld syndrome Orphanet:782 ICD9:743.44 Axenfeldt-Rieger syndrome MESH:C535679 iridogoniodysgenesis with somatic anomalies NORD:1670 UMLS:C3495488 SCTID:47507006 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. OMIMPS:180500 goniodysgenesis hypodontia MedDRA:10059255 DOID:14686 MONDO:0019187 neurocristopathy ocular growth disorder