All diseases

10 entries on 1 page. Showing entries 1 - 10.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00904 ALSG aplasia of lacrimal and salivary glands (ALSG) 180920 AD 5 5 FGF10 - -
03629 EMARDD myopathy, areflexia, respiratory distress, and dysphagia, early-onset 614399 AR - 1 MEGF10 - -
01780 F10D deficiency, factor X (F10D) 227600 AR - 1 F10 - -
01817 GA3 Glutaric aciduria III 231690 AR - - C7orf10 - -
02107 HNSCC carcinoma, squamous cell, head and neck (HNSCC) 275355 AR 5 5 ING1, PTEN, TNFRSF10B - -
06035 IBD29 {Inflammatory bowel disease 29} 618077 AD - - C1orf106 - -
00599 LADD lacrimoauriculodentodigital syndrome - AD 9 9 FGF10, FGFR2, FGFR3 - -
07090 LADD3 lacrimoauriculodentodigital syndrome, type 3 620193 AD - - FGF10 - -
05905 SHDRA heart defects, structural, and renal anomalies syndrome (SHDRA) 617478 AR - - C14orf101 - -
02747 SNCV nerve conduction velocity, slowed, autosomal dominant (SNCV) 608236 AD 1 1 ARHGEF10 - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.