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DOID:0110138 - Bardet-Biedl syndrome 16
Disease Ontology Definition:A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutations in the SDCCAG8 gene on chromosome 1q43.
Synonyms: BBS16
Xenbase Genes
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			sdccag8
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			sdccag8
			
			
		
		
			
						
		
		
	| MONDO:0014444 - Bardet-Biedl syndrome 16 | 
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): 
			
				
					Bardet-Biedl syndrome (is_a)
				
				
			
		
		