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
03527 CDCBM1 dysplasia ,cortical, complex, with other brain malformations (CDCBM-1) 614039 AD 5 5 TUBB3 - -
05050 CFEOM3A fibrosis of extraocular muscles, congenital, type 3A (CFEOM-3A) 600638 AD 1 1 TUBB3 - -
Legend   How to query  


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