All diseases

1 entry on 1 page. Showing entry 1.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05566 SPGF20 spermatogenic failure, type 18 (SPGF-20) 617593 AR - - WDR52 - autosomal recessive
Legend   How to query  


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