All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00089 DFNB97 Deafness, autosomal recessive 97 616705 - 0 0 MET - -
00091 OSFD Osteofibrous dysplasia, susceptibility to 607278 - 0 0 MET - -
00090 RCCP1 Renal cell carcinoma, papillary, 1 605074 - 0 0 MET kidney -
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