All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05557 ALS25 sclerosis, lateral, amyotrophic, type 25 (ALS25) 617921 AD - - KIF5A - autosomal dominant
05556 NEIMY myoclonus, intractable, neonatal (NEIMY) 617235 AD - - KIF5A - autosomal dominant
00213 SPG10 paraplegia, spastic, autosomal dominant, type 10 (SPG-10) 604187 AD 8 7 KIF5A - -
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