dcGO - A comprehensive domain-centric ontology resource for post-genomic research on functions, phenotypes, diseases and more   
  
  

Phenotypic Abnormality (PA): Leukemia

(show info)

Jump to [ Top · Hierarchy · Annotations ]

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:   Neoplasm [HP:0002664] <2>(18|17) (23|7|2)
+ + + 3:   Abnormality of the immune system [HP:0002715] <3>(31|42) (36|27|14)
+ + + 3:   Phenotypic abnormality [HP:0000118] <26>
+ + 2:   Abnormality of blood and blood-forming tissues [HP:0001871] <10>(20|31) (27|15|5)
+ + 2:   Abnormality of cellular immune system [HP:0010987] <1>(5|10) (6|5|2)
+ + 2:   Neoplasm by anatomical site [HP:0011793] <24>(16|15) (20|7|2)
+ 1:   Abnormal leukocyte morphology [HP:0001881] <5>(5|10) (6|5|2)
+ 1:   Hematological neoplasm [HP:0004377] <7>(3|2) (3|2|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)