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DOID:0050572 - cone-rod dystrophy
Disease Ontology Definition:A retinal degeneration that characterized by progressive deterioration of the cone and rod photoreceptor cells.
Synonyms: cone-rod retinal dystrophy
Xenbase Genes
 :
		
					
			
			rab28,
			
			
		
		
			
						
		
					
			
			crx,
			
			
		
		
			
						
		
					
			
			cdhr1,
			
			
		
		
			
						
		
					
			
			rax2,
			
			
		
		
			
						
		
					
			
			prom1,
			
			
		
		
			
						
		
					
			
			poc1b,
			
			
		
		
			
						
		
					
			
			cnga3,
			
			
		
		
			
						
		
					
			
			unc119,
			
			
		
		
			
						
		
					
			
			opn1lw,
			
			
		
		
			
						
		
					
			
			cfap410,
			
			
		
		
			
						
		
					
			
			rlbp1,
			
			
		
		
			
						
		
					
			
			adam9,
			
			
		
		
			
						
		
					
			
			rpgr,
			
			
		
		
			
						
		
					
			
			pitpnm3,
			
			
		
		
			
						
		
					
			
			atf6,
:
		
					
			
			rab28,
			
			
		
		
			
						
		
					
			
			crx,
			
			
		
		
			
						
		
					
			
			cdhr1,
			
			
		
		
			
						
		
					
			
			rax2,
			
			
		
		
			
						
		
					
			
			prom1,
			
			
		
		
			
						
		
					
			
			poc1b,
			
			
		
		
			
						
		
					
			
			cnga3,
			
			
		
		
			
						
		
					
			
			unc119,
			
			
		
		
			
						
		
					
			
			opn1lw,
			
			
		
		
			
						
		
					
			
			cfap410,
			
			
		
		
			
						
		
					
			
			rlbp1,
			
			
		
		
			
						
		
					
			
			adam9,
			
			
		
		
			
						
		
					
			
			rpgr,
			
			
		
		
			
						
		
					
			
			pitpnm3,
			
			
		
		
			
						
		
					
			
			atf6,
			
			
		
		
							
							
				
	| MONDO:0015993 - cone-rod dystrophy | 
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): 
			
				
					monogenic disease (is_a), 
				
				
			
				
					retinal degeneration (is_a)
				
				
			
		
		