All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00332 CILD dyskinesia, ciliary, primary (CILD) - - 219 211 C21orf59, CCDC164, CCDC39, DNAAF3, DNAH1, DNAH5, HEATR2, HYDIN, TTC12 - -
05980 CILD37 dyskinesia, ciliary, primary, type 37 (CILD37) 617577 AR - - DNAH1 - -
03071 CILD7 dyskinesia, ciliary, primary, 7 (CILD-7) 611884 AR 1 1 DNAH11 - -
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 - -
05561 SPGF18 spermatogenic failure, type 18 (SPGF18) 617576 AR - - DNAH1 - autosomal recessive
06384 SPGF39 Spermatogenic failure 39 618643 AR - - DNAH17 - -
06925 SPGF56 spermatogenic failure, type 56 619515 AR - - DNAH10 - -
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