All diseases

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05311 LFIT2 failure, liver, transient, infantile, type 2 (LFIT-2) 616483 AR 1 - NBAS - -
03727 SOPH stature, short, optic nerve atrophy, and pelger-huet anomaly (SOPH) 614800 AR 1 1 NBAS - -
Legend   How to query  


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