All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04212 BBS Bardet-Biedl syndrome (BBS) - - 282 240 ARL6, BBS9, C8orf37, IFT74 - -
06811 BBS20 Bardet-Biedl syndrome, type 20 617119 AR - - IFT74 - -
05562 SPGF spermatogenic failure (SPGF) - - 96 94 ACRC, AURKC, C14orf39, C15orf43, CCDC62, CFAP58, DNAH1, DNAH2, DNALI1, DPY19L2, FANCM, FBXO43, GGN, IFT74, MEIOB, PDHA2, PLCZ1, PNLDC1, RNF212, RPL10L, 6 more - -
06923 SPGF58 spermatogenic failure, type 58 619585 AR - - IFT74 - -
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