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
06998 ALS26 sclerosis, lateral, amyotrophic, with/without frontotemporal dementia, type 26 619133 AD - - TIA1 - -
00109 WDM myopathy, distal, Welander (WDM) 604454 AD;AR 1 2 TIA1 - -
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