All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02094 TTP thrombocytopenic purpura, thrombotic, congenital (TTP, Upshaw-Schulman syndrome) 274150 AR 50 0 ADAMTS13 - -
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