All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03526 - Emberger syndrome 614038 AD 8 8 GATA2 - -
00908 AML leukemia, myeloid, acute (AML) 601626 - 43 28 CBFB, CEBPA, CHIC2, ETV6, FLT3, GATA2, JAK2, KIT, KRAS, LPP, MLF1, MLLT10, NPM1, NSD1, NUP214, PICALM, PTPN11, RUNX1, SH3GL1, TERT, WHSC1L1 - -
03571 IMD21 Immunodeficiency 21 614172 AD 21 1 GATA2 - -
00132 MDS myelodysplastic syndrome (MDS) 614286 SMo 10 13 ASXL1, GATA2, PTPN11, SF3B1, TET2 - -
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