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
04569 CMT2U Charcot-Marie-Tooth disease, axonal, type 2U (CMT-2U) 616280 AD 2 2 MARS - -
04570 COXPD25 oxidative phosphorylation deficiency?, combined, type 25 (COXPD-25) 616430 AR - - MARS2 - -
03964 ILLD lung and liver disease, interstitial (ILLD, liver failure syndrome, infantile, type 2) 615486 AR 7 7 MARS - -
03025 SPAX3 ataxia, spastic, type 3, autosomal dominant (SPAX-3) 611390 AR - - MARS2 - -
Legend   How to query  


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