All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03939 IBMPFD2 myopathy, inclusion body, with early-onset Paget disease with/without frontotemporal dementia, type 2 (IBMPFD-2) 615422 - - - HNRNPA2B1 - -
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