				Excel File Text File All mouse models of Pendred Syndrome with phenotypic similarity to the human disease
				Disease Term	Allelic Composition	Genetic Background	Reference	Phenotypes
				Pendred Syndrome	Slc26a4em1Jgao/Slc26a4em1Jgao	involves: CBA/CaJ	J:291230	View
				Pendred Syndrome	Slc26a4pdsm/Slc26a4pdsm	BXA7/PgnJ-Slc26a4^pdsm/J	J:121997	View
				Pendred Syndrome	Slc26a4tm1Egr/Slc26a4tm1Egr	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	J:67072	View
				Pendred Syndrome	Slc26a4tm1Egr/Slc26a4tm1Egr	involves: 129S6/SvEvTac	J:116301, J:101834, J:121442	View
				Pendred Syndrome	Foxi1tm1Sven/Foxi1tm1Sven	involves: CD-1	J:83207	View

				No similarity to the expected human disease phenotype was found.
				Disease Term	Allelic Composition	Genetic Background	Reference	Phenotypes
NOT Models				Pendred Syndrome	Slc26a4tm2.1Dontu/Slc26a4tm2.1Dontu	B6.129-Slc26a4^tm2.1Dontu	J:203206	View