Disease #00908 (AML (leukemia, myeloid, acute (AML)), OMIM:601626)
Official abbreviation |
AML |
Name |
leukemia, myeloid, acute (AML) |
OMIM ID |
601626 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
43 |
Phenotype entries for this disease |
28 |
Associated with 21 genes |
CBFB, CEBPA, CHIC2, ETV6, FLT3, GATA2, JAK2, KIT, KRAS, LPP, MLF1, MLLT10, NPM1, NSD1, NUP214, PICALM, PTPN11, RUNX1, SH3GL1, TERT, WHSC1L1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2015-12-08 23:50:05 +01:00 (CET) |
Individuals
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