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CTD Diseases (CD): Leukemia, Myeloid, Acute

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Root: CD Hierarchy (CTD diseases from Comparative Toxicogenomics Database)

Shortest distance to current term
(+ for parents, - for children)
CD term [CD ID] <#Children> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   Diseases [MESH:C] <27>
+ + + + 4:   Neoplasms [MESH:D009369] <17>(0|0) (0|0|0)
+ + + 3:   Neoplasms by Histologic Type [MESH:D009370] <14>(0|0) (0|0|0)
+ + 2:   Leukemia [MESH:D007938] <11>(0|0) (0|0|0)
+ 1:   Leukemia, Myeloid [MESH:D007951] <9>(0|0) (0|0|0)
0:   Leukemia, Myeloid, Acute [MESH:D015470] <13>(0|0) (0|0|0)
- 1:   Leukemia, Erythroblastic, Acute [MESH:D004915] <1>(0|0) (0|0|0)
- 1:   Leukemia, Megakaryoblastic, Acute [MESH:D007947] <1>(0|0) (0|0|0)
- 1:   Dohle Bodies and Leukemia [MESH:C565617](0|0) (0|0|0)
- 1:   Erythroleukemia, Familial [MESH:C565039](0|0) (0|0|0)
- 1:   Familial Acute Myeloid Leukemia with Mutated Cebpa [MESH:C580075](0|0) (0|0|0)
- 1:   Leukemia, Acute Myelocytic, with Polyposis Coli and Colon Cancer [MESH:C565441](0|0) (0|0|0)
- 1:   Leukemia, Basophilic, Acute [MESH:D015471](0|0) (0|0|0)
- 1:   Leukemia, Eosinophilic, Acute [MESH:D015472](0|0) (0|0|0)
- 1:   Leukemia, Mast-Cell [MESH:D007946](0|0) (0|0|0)
- 1:   Leukemia, Monocytic, Acute [MESH:D007948](0|0) (0|0|0)
- 1:   Leukemia, Promyelocytic, Acute [MESH:D015473](0|0) (0|0|0)
- 1:   Monosomy 7 of Bone Marrow [MESH:C565370](0|0) (0|0|0)
- 1:   Platelet Disorder, Familial, with Associated Myeloid Malignancy [MESH:C563324](0|0) (0|0|0)