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MIRAGE
acute myeloid leukemia
Summary
- Synonym
-
- AML - acute Myeloid Leukemia
- Leukemia, Myelocytic, acute
- acute myeloblastic leukaemia
- acute myeloblastic leukemia
- acute myelogenous leukaemia
- acute myelogenous leukemia
- acute myeloid leukaemia
- Definition
- A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells.
- Super Class
- myeloid leukemia
External Links
- Disease Ontology
- DOID:9119
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 8301 | PICALM | phosphatidylinositol binding clathrin assembly protein | |
| 10499 | NCOA2 | nuclear receptor coactivator 2 | |
| 23305 | ACSL6 | acyl-CoA synthetase long chain family member 6 | |
| 25939 | SAMHD1 | SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 | |
| 29117 | BRD7 | bromodomain containing 7 | |
| 54790 | TET2 | tet methylcytosine dioxygenase 2 | |
| 64324 | NSD1 | nuclear receptor binding SET domain protein 1 | |
| 84295 | PHF6 | PHD finger protein 6 | |
| 171023 | ASXL1 | ASXL transcriptional regulator 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P04637 | Cellular tumor antigen p53 | |
| P04798 | Cytochrome P450 1A1 | |
| P04818 | Thymidylate synthase | |
| P05106 | Integrin beta-3 | |
| P05231 | Interleukin-6 | |
| P06748 | Nucleophosmin | |
| P06756 | Integrin alpha-V | |
| P09919 | Granulocyte colony-stimulating factor | |
| P10721 | Mast/stem cell growth factor receptor Kit | |
| P11245 | Arylamine N-acetyltransferase 2 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| P45481 | Histone lysine acetyltransferase CREBBP | |
| P55200 | Histone-lysine N-methyltransferase 2A | |
| P59598 | Polycomb group protein ASXL1 | |
| Q00342 | Receptor-type tyrosine-protein kinase FLT3 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| P49687 | Nucleoporin NUP145 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001442 | Typified by somatic mosaicism |
| HP:0000006 | Autosomal dominant inheritance |
| HP:0004808 | Acute myeloid leukemia |
