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
00904 - Aplasia of lacrimal and salivary glands 180920 - - - FGF10 - -
01817 - Glutaryl-CoA oxidase deficiency 231690 - - - C7orf10 - -
03629 - myopathy, areflexia, respiratory distress, and dysphagia, early-onset 614399 - - - MEGF10 - -
01780 F10D factor X deficiency (F10D) 227600 - - - F10 - -
02107 HNSCC carcinoma, squamous cell, head and neck (HNSCC) 275355 - - - ING1, PTEN, TNFRSF10B - -
00599 LADD lacrimoauriculodentodigital syndrome ((LADD), Levy-Hollister) 149730 - - - FGF10, FGFR2, FGFR3 - -
02747 SNCV nerve conduction velocity, slowed, autosomal dominant (SNCV) 608236 - - - ARHGEF10 - -
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