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
03336 - dysplasia, frontonasal, type 2 613451 AR - - ALX4 - -
03990 CRS5 craniosynostosis, type 5, susceptibility to (CRS-5) 615529 AD - - ALX4 - -
02861 PFM2 foramina, parietal, type 2 (PFM-2) 609597 AD - - ALX4 - -
Legend   How to query  


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