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Mammalian Phenotype (MP): abnormal hematopoietic stem cell proliferation

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Root: MP Hierarchy (mammalian/mouse phenotype from MGI_4.41)

Shortest distance to current term (+ for parents, - for children) MP term [MP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + 3:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + 2:   abnormal hematopoietic system physiology [MP:0001545] <5>(39|53) (40|38|21)
+ + 2:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ 1:   abnormal hematopoietic stem cell physiology [MP:0010763] <2>(0|0) (0|0|0)
+ 1:   abnormal cell proliferation [MP:0000350] <31>(15|19) (18|11|5)
0:   abnormal hematopoietic stem cell proliferation [MP:0011901] <2>(0|0) (0|0|0)
- 1:   decreased hematopoietic stem cell proliferation [MP:0011903](0|0) (0|0|0)
- 1:   increased hematopoietic stem cell proliferation [MP:0011902](0|0) (0|0|0)