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
00456 ALS-1 sclerosis, lateral, amyotrophic, type 1 (ALS-1) 105400 - 6 6 DCTN1, NEFH, PRPH, SOD1 - -
00454 HMN-7B neuropathy, motor, distal, hereditary, type VIIb (HMN-7B) 607641 - 0 0 DCTN1 - -
00453 Perry Perry syndrome 168605 - 8 8 DCTN1 - -
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