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ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00160	500004	RETINITIS PIGMENTOSA-DEAFNESS SYNDROME	500004	0	0	CDH23, CLRN1, DFNB31, GPR98, MT-TS2, MYO7A, PCDH15, USH1C, USH1G, USH2A	-	-

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