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
03706 ALS17 sclerosis, lateral, amyotrophic, type 17 (ALS17) 614696 AD 4 - CHMP2B - -
02314 FTD3 dementia, frontotemporal, chromosome 3-linked (FTD-3) 600795 AD - - CHMP2B - -
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