All diseases

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04255 ALS sclerosis, lateral, amyotrophic (ALS) - - 471 442 GLE1, LRP12, PFN1 - -
00026 arthrogryposis arthrogryposis - - 60 60 GLE1, TNNT3 - -
00008 CAAHD arthrogryposis, lethal, with anterior horn cell, congenital (CAAHD) 611890 AR 18 16 GLE1 - -
00007 LCCS1 contracture syndrome, lethal, congenital, type 1 253310 AR 32 33 GLE1 - -
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