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
00033 AML Acute Myeloid Leukemia 601626 - 5 5 CEBPA, GATA2, KIT, NSD1, RUNX1 bone marrow -
00133 FPDMM Platelet disorder, familial, with associated myeloid malignancy 601399 - 0 0 RUNX1 - -
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