All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
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 - -
02222 CPDX2 chondrodysplasia punctata, type 2, X-linked dominant (CPDX-2, Conradi-Hunermann syndrome) 302960 XLD 30 30 EBP - -
06758 EDSCLL2 Ehlers-Danlos syndrome, classic-like, 2 618000 AR 2 2 AEBP1 - -
06846 MEND MEND syndrome 300960 XLR - - EBP - -
01888 SGD1 Specific granule deficiency 245480 AR - - CEBPE - -
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