All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05400 DFNB deafness, autosomal recessive (DFNB) - - 977 972 CDH23, CIB2, FAM65B, GIPC3, GRXCR1, HGF, MYO15A, MYO7A, OTOF, OTOG, PCDH15, RDX, S1PR2, SERPINB6, STRC, TMC1, USH1C - autosomal recessive
05410 DFNB68 deafness, autosomal recessive, type 68 (DFNB-68) 610419 AR - - S1PR2 - autosomal recessive
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