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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Neoplasm [HP:0002664] <2>(22|19) (23|4|3)
+ + + 3:   Abnormality of the immune system [HP:0002715] <3>(32|44) (35|27|13)
+ + 2:   Neoplasm by anatomical site [HP:0011793] <24>(19|18) (20|4|3)
+ + 2:   Abnormality of cellular immune system [HP:0010987] <1>(1|7) (3|3|0)
+ + 2:   Abnormality of blood and blood-forming tissues [HP:0001871] <11>(21|32) (27|14|3)
+ 1:   Abnormal leukocyte morphology [HP:0001881] <5>(1|7) (3|3|0)
+ 1:   Hematological neoplasm [HP:0004377] <7>(3|3) (4|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)