All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00148 DFNA17 deafness, autosomal dominant, type 17 (DFNA-17) 603622 AD - - MYH9 - autosomal dominant
00145 ESS Epstein syndrome (ESS) 153650 - - - MYH9 - -
00144 FTNS Fechtner syndrome (FTNS) 153640 - - - MYH9 - -
00146 MATINS;MHA;BDPLT6 macrothrombocytopenia, granulocyte inclusions with/without nephritis or sensorineural hearing loss (MATINS, May-Hegglin anomaly (MHA), bleeding disorder platelet type 6 (BDPLT-6)) 155100 AD 37 36 MYH9 - autosomal dominant
00147 MTCPSD macrothrombocytopenia and progressive sensorineural deafness (MTCPSD) 600208 - - - MYH9 - -
00149 SBS Sebastian syndrome (SBS) 605249 - - - MYH9 - -
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