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Phenotypic Abnormality (PA): Leukemia

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term
(+ for parents, - for children)
HP term [HP ID] <#Children> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   Abnormality of the immune system [HP:0002715] <3>(35|48) (38|27|14)
+ + + 3:   Neoplasm [HP:0002664] <2>(20|22) (24|7|4)
+ + + 3:   Abnormal immune system morphology [HP:0032251] <3>(9|11) (9|6|2)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Neoplasm by anatomical site [HP:0011793] <24>(19|19) (22|6|3)
+ + 2:   Abnormal cellular immune system morphology [HP:0010987] <1>(8|10) (8|6|2)
+ + 2:   Abnormality of blood and blood-forming tissues [HP:0001871] <11>(23|36) (27|16|5)
+ 1:   Abnormal leukocyte morphology [HP:0001881] <4>(5|10) (7|5|2)
+ 1:   Hematological neoplasm [HP:0004377] <7>(2|3) (3|1|0)
0:   Leukemia [HP:0001909] <5>(0|0) (0|0|0)
- 1:   Acute leukemia [HP:0002488] <7>(0|0) (0|0|0)
- 1:   Myeloid leukemia [HP:0012324] <3>(0|0) (0|0|0)
- 1:   Chronic leukemia [HP:0005558] <2>(0|0) (0|0|0)
- 1:   Lymphoid leukemia [HP:0005526] <1>(0|0) (0|0|0)
- 1:   Myeloproliferative disorder [HP:0005547] <1>(0|0) (0|0|0)