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
00456 ALS1 sclerosis, lateral, amyotrophic, type 1 (ALS1) 105400 AD;AR 6 6 DCTN1, NEFH, PRPH, SOD1 - -
06538 CMT2CC Charcot-Marie-Tooth disease, axonal, type 2CC 616924 AD - - NEFH - -
Legend   How to query  


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