Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Axenfeld-Rieger syndrome

MONDO:0019187

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.

Also known as: ARS, Axenfeld syndrome, Axenfeldt-Rieger syndrome, Rieger syndrome, goniodysgenesis hypodontia, iridogoniodysgenesis with somatic anomalies

1 clinical trial for this condition and its sub-types, 1 tagged with Axenfeld-Rieger syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by