All diseases

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03870 HH17 hypogonadism, hypogonadotropic, type 17 with/without anosmia (HH-17) 615266 AD - - SPRY4 - -
06215 IGAN3 {?IgA nephropathy, susceptibility to, 3} 616818 AD - - SPRY2 - -
05193 SEMDFA dysplasia, spondylopeimetaphyseal, Faden-Alkuraya type (SEMDFA) 616723 AR 1 1 RSPRY1 - -
Legend   How to query  


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