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
06917 OZEMA12;OOMD ocyte/zygote/embryo maturation arrest, type 12 - AR - - FBXO43 - -
05450 OZEMA;OOMD ocyte/zygote/embryo maturation arrest - - 38 40 FBXO43, PANX1, PATL2, TUBB8, ZP1, ZP3 - -
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 - -
06916 SPGF64 spermatogenic failure, type 64 619696 AR - - FBXO43 - -
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