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
03493 ALS14 sclerosis, lateral, amyotrophic, type 14, with/without frontotemporal dementia (ALS14) 613954 - 0 0 VCP - -
06808 CMT2Y Charcot-Marie-Tooth disease, type 2Y 616687 AD 0 0 VCP - -
00218 IBMPFD myopathy, inclusion body, with early-onset Paget disease and frontotemporal dementia (IBMPFD) 167320 AD 62 20 VCP - -
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