Axenfeld-Rieger syndrome
MONDO:0019187Axenfeld-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.
Also known as: ARS, Axenfeld syndrome, Axenfeldt-Rieger syndrome, Rieger syndrome, goniodysgenesis hypodontia, iridogoniodysgenesis with somatic anomalies
14 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Broader categories
Disease
(618)
Hereditary disease
(172)
Eye disorder
(97)
Syndromic disease
(24)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Disorder of orbital region
(3)
Disease of genetic or genomic mechanism
(2)
Disorder of visual system
(1)
Multiple congenital anomalies/dysmorphic syndrome
(1)