All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05458 DFN deafness, nonsyndromic (DFN) - - 49 44 CDC14A, CDH23, CEACAM16, FAM65B, MYO15A, MYO6, MYO7A, OTOF, OTOG, PCDH15, PDZD7, TECTA, TMC1, USH1C - -
05400 DFNB deafness, autosomal recessive (DFNB) - - 955 951 CDH23, CIB2, FAM65B, GRXCR1, HGF, MYO15A, MYO7A, OTOF, OTOG, PCDH15, RDX, S1PR2, SERPINB6, STRC, TMC1, USH1C - autosomal recessive
02357 DFNB12 deafness, autosomal recessive, type 12 (DFNB-12) 601386 AR 6 6 ATP2B2, CDH23 - -
06082 PITA5 {Pituitary adenoma 5, multiple types} 617540 AD - - CDH23 - -
05415 USH Usher syndrome (USH) - - 457 455 ARSG, CDH23, CIB2, CLRN1, GPR98, MYO7A, PCDH15, USH1C, USH1G, USH2A - -
02115 USH1 Usher syndrome, type I (USH-1) - - 644 645 CDH23, MYO7A, PCDH15, USH1C, USH1G - -
02337 USH1D Usher syndrome, type 1D (USH-1D) 601067 AR;DR 1 - CDH23 - -
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