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
03942 ALS-20 sclerosis, lateral, amyotrophic, type 20 (ALS-20) 615426 - 0 0 HNRNPA1 - -
03940 IBMPFD-3 myopathy, inclusion body, with early-onset Paget disease with or without frontotemporal dementia, type 3 (IBMPFD-3) 615424 - 0 0 HNRNPA1 - -
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