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
00908 AML leukemia, myeloid, acute (AML) 601626 - - - CBFB, CEBPA, CHIC2, ETV6, FLT3, GATA2, JAK2, KIT, KRAS, LPP, MLF1, MLLT10, NPM1, NSD1, NUP214, PICALM, RUNX1, SH3GL1, TERT, WHSC1L1 - -
03558 DFNB-81;PRLTS-3 deafness, autosomal recessive, type 81 (DFNB-81, Perrault syndrome, type 3 (PRLTS-3)) 614129 - - - CLPP - -
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