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
00332 CILD dyskinesia, ciliary, primary (CILD) - - 219 211 C21orf59, CCDC164, CCDC39, DNAAF3, DNAH1, DNAH5, HEATR2, HYDIN, TTC12 - -
06154 CILD45 Ciliary dyskinesia, primary, 45 618801 AR - - TTC12 - -
05452 MC3DN mitochondrial complex III deficiency, nuclear (MC3DN)] - - 4 4 BCS1L, C11orf83, CYC1, LYRM7, MNF1, TTC19, UQCRB, UQCRC2, UQCRFS1, UQCRQ - -
03842 MC3DN2 mitochondrial complex III deficiency, nuclear type 2 (MC3DN-2) 615157 AR 4 4 TTC19 - -
06098 SPGF41 ?Spermatogenic failure 41 618670 AR - - TTC18 - -
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