Preferred Label : Rieger-Axenfeld anomaly;
ICD-11 definition : 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
(mild craniofacial dysmorphism, dental anomalies and redundant periumbilical skin).;
Origin ID : 1338180594;
Automatic exact mappings (from CISMeF team)
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
(mild craniofacial dysmorphism, dental anomalies and redundant periumbilical skin).
