All diseases associated with gene SPG11

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated tissues

Disease features
06256 ALS5 Amyotrophic lateral sclerosis 5, juvenile 602099 AR - - - -
06260 CMT2X Charcot-Marie-Tooth disease, axonal, type 2X 616668 AR - - - -
00325 SPG paraplegia, spastic (SPG) - - 127 121 - -
02501 SPG11 paraplegia, spastic, autosomal recessive, type 11 (SPG-11) 604360 AR 39 37 - -
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