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Mammalian Phenotype (MP): abnormal spleen primary B follicle morphology

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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)
+ + + + + + + 7:   mammalian phenotype [MP:0000001] <29>
+ + + + + + 6:   immune system phenotype [MP:0005387] <2>(76|114) (86|66|35)
+ + + + + 5:   abnormal immune system morphology [MP:0000685] <3>(50|76) (60|35|18)
+ + + + + 5:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + + + 4:   abnormal immune system organ morphology [MP:0002722] <8>(21|31) (26|15|9)
+ + + + 4:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(57|86) (66|47|21)
+ + + 3:   abnormal spleen morphology [MP:0000689] <16>(10|15) (12|8|8)
+ + 2:   abnormal spleen white pulp morphology [MP:0002357] <10>(6|8) (6|6|3)
+ 1:   abnormal spleen B cell follicle morphology [MP:0008470] <3>(4|6) (4|4|2)
0:   abnormal spleen primary B follicle morphology [MP:0008471](0|0) (0|0|0)