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
02357 DFNB-12 deafness, autosomal recessive, type 12 (DFNB-12) 601386 - - - ATP2B2, CDH23 - -
02337 USH-1D Usher syndrome, type 1D (USH-1D) 601067 - - - CDH23, PCDH15 - -
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