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Axenfeld-Rieger syndrome
rareAxenfeld-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.
- Identifiers
- MONDO:0019187 Orphanet:782
- Part of
- Hereditary diseaseMultiple congenital anomalies/dysmorphic syndrome without intellectual disabilityNeurocristopathyOcular growth disorderSyndromic disease
- Also known as
- ARS · Axenfeld syndrome · Axenfeldt-Rieger syndrome · goniodysgenesis hypodontia · iridogoniodysgenesis with somatic anomalies
Subtypes
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