All diseases

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00169 EDS Ehlers-Danlos syndrome (EDS) - - 1800 241 ADAMTS2, B4GALT7, COL1A1, COL1A2, COL3A1, COL5A1, COL5A2, FKBP14, PLOD1, PRDM5, SLC39A13, TNXB - -
02585 EDSCLL Ehlers-Danlos-like syndrome, classic-like type (EDSCLL) 606408 AR 28 14 TNXB - -
01301 EDSHMB Ehlers-Danlos syndrome, hypermobility type (EDSHMB, EDS3) 130020 - 25 3 TNXB - -
05039 VUR8 reflux, vesicoureteral, type 8 (VUR8) 615963 AD 9 - TNXB - -
Legend   How to query  


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