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
04188 ODG dysgenesis, ovarian (ODG) - - - - ESR2, SOHLH1 - -
05856 ODG5 dysgenesis, ovarian, type 5 (ODG5) 617690 AR - - SOHLH1 - -
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 - -
05857 SPGF32 spermatogenic failure, type 32 (SPGF32) 618115 AD - - SOHLH1 - -
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