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
02191 AUTSX5 autism, susceptibility to, X-linked, type 5 (AUTSX-5) 300847 - - - RPL10 - -
05325 MRXS35 mental retardation, X-linked, syndromic, type 35 (MRXS-35) 300998 XLR 1 1 RPL10 - -
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 - -
06918 SPGF63 spermatogenic failure, type 63 619689 AR - - RPL10L - -
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