All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05895 INF infertility - - 20 19 C14orf39, C9orf84 - -
04187 POF ovarian failure, premature (POF) - - 37 22 C14orf39, FOXL2, HFM1, MCM8, NOBOX, STAG3, SYCP2L - -
06898 POF18 ovarian failure, premature, type 18 619203 AR - - C14orf39 - -
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 - -
06897 SPGF52 spermatogenic failure, type 52 619202 AR - - C14orf39 - -
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