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
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 - -
03837 CMM-9 melanoma, cutaneous, malignant, susceptibility to, type 9 (CMM-9) 615134 - - - TERT - -
03510 DKCA-2;DCKB-4 dyskeratosis congenita, autosomal dominant, type 2 (DKCA-2, autosomal recessive (DKCB-4)) 613989 - - - TERT - -
03718 PFBMFT-1 fibrosis, pulmonary, and/or bone marrow failure, telomere-related, type 1 (PFBMFT-1) 614742 - - - TERT - -
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