All diseases

8 entries on 1 page. Showing entries 1 - 8.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01817 - Glutaryl-CoA oxidase deficiency 231690 - 0 0 C7orf10 - -
03629 - myopathy, areflexia, respiratory distress, and dysphagia, early-onset 614399 - 0 1 MEGF10 - -
00904 ALSG aplasia of lacrimal and salivary glands (ALSG) 180920 AD 5 5 FGF10 - -
01780 F10D deficiency, factor X (F10D) 227600 - 0 0 F10 - -
02107 HNSCC carcinoma, squamous cell, head and neck (HNSCC) 275355 - 4 4 ING1, PTEN, TNFRSF10B - -
00599 LADD syndrome, LADD (lacrimoauriculodentodigital, Levy-Hollister) 149730 AD 7 7 FGF10, FGFR2, FGFR3 - -
05905 SHDRA heart defects, structural, and renal anomalies syndrome (SHDRA) 617478 AR 0 0 C14orf101 - -
02747 SNCV nerve conduction velocity, slowed, autosomal dominant (SNCV) 608236 - 1 1 ARHGEF10 - -
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