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
02697 - Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive 607706 AR 4 3 GDAP1 - -
02709 CMT2K Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2K 607831 AD;AR 7 5 GDAP1, JPH1 - -
01705 CMT4A Charcot-Marie-Tooth disease, type 4A (CMT-4A) 214400 AR 25 25 GDAP1 - -
02752 CMTRIA Charcot-Marie-Tooth disease, recessive intermediate A (CMTRIA) 608340 AR - - GDAP1 - -
Legend   How to query  


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