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DOID:14686 - Axenfeld-Rieger syndrome
Disease Ontology Definition:An eye disease characterized by abnormalities of the front part of the eye, the anterior segment.
Synonyms: Anomaly, Rieger's, Axenfeld syndrome, Axenfeld syndrome , Hagedoom syndrome, RGS - Rieger syndrome, Rieger's anomaly
Xenbase Genes
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			foxc1,
			
			
		
		
			
						
		
					
			
			pitx2
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			foxc1,
			
			
		
		
			
						
		
					
			
			pitx2
			
			
		
		
			
						
		
		
	| MONDO:0019187 - Axenfeld-Rieger syndrome | 
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): 
			
				
					autosomal dominant disease (is_a), 
				
				
			
				
					eye disease (is_a)
				
				
			
		
		