All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03617 ALS16 sclerosis, lateral, amyotrophic, type 16, juvenile (ALS16) 614373 AR - - SIGMAR1 - -
07241 HMNR2;DSMA2 neuronopathy, distal hereditary motor, autosomal recessive, type 2 605726 AR - - SIGMAR1 - -
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