All diseases

4 entries on 1 page. Showing entries 1 - 4.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00026 - arthrogryposis, congenital - 4 5 GLE1 - -
04255 ALS sclerosis, lateral, amyotrophic (ALS) - 18 18 GLE1 - -
00008 LAAHD arthrogryposis, lethal, with anterior horn cell disease (LAAHD) 611890 1 38 GLE1 - -
00007 LCCS-1 contracture syndrome, lethal, congenital, type 1 (LCCS-1) 253310 3 5 GLE1 - -