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
06722 NEDALVS Neurodevelopmental disorder with absent language and variable seizures 618707 AD - - WASF1 - -
02146 SCNX neutropenia, congenital, severe, X-linked (SCNX) 300299 XLR - - WAS - -
02268 THC1;XLT thrombocytopenia, type 1 (THC-1, thrombocytopenia X-linked (XLT)) 313900 XLR - - WAS - -
05061 WAS Wiskott-Aldrich syndrome (WAS) 301000 XLR 2 2 WAS - -
Legend   How to query  


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