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Mammalian Phenotype (MP): abnormal T-helper 17 cell 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)
+ + + + + + + + + + + 11:   mammalian phenotype [MP:0000001] <29>
+ + + + + + + + + + 10:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + + + + + + + + + 10:   immune system phenotype [MP:0005387] <2>(76|114) (86|66|35)
+ + + + + + + + + 9:   abnormal immune system morphology [MP:0000685] <3>(50|76) (60|35|18)
+ + + + + + + + + 9:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(57|86) (66|47|21)
+ + + + + + + + 8:   abnormal hematopoietic cell morphology [MP:0013656] <9>(48|77) (60|43|18)
+ + + + + + + + 8:   abnormal immune system cell morphology [MP:0000716] <5>(37|63) (48|29|16)
+ + + + + + + 7:   abnormal leukocyte morphology [MP:0008246] <4>(36|62) (47|29|15)
+ + + + + + 6:   abnormal mononuclear cell morphology [MP:0008247] <2>(33|57) (41|28|14)
+ + + + + 5:   abnormal lymphocyte morphology [MP:0002619] <5>(27|46) (33|26|14)
+ + + + 4:   abnormal T cell morphology [MP:0008037] <9>(14|25) (18|19|11)
+ + + 3:   abnormal alpha-beta T cell morphology [MP:0012762] <13>(7|17) (8|14|6)
+ + + 3:   abnormal effector T cell morphology [MP:0002435] <7>(7|16) (8|13|6)
+ + 2:   abnormal CD4-positive, alpha beta T cell morphology [MP:0002432] <6>(3|11) (4|10|4)
+ + 2:   abnormal T-helper cell morphology [MP:0013760] <2>(0|1) (0|0|0)
+ 1:   abnormal CD4-positive helper T cell morphology [MP:0010183] <4>(0|1) (0|0|0)
0:   abnormal T-helper 17 cell morphology [MP:0010217] <2>(0|1) (0|0|0)
- 1:   abnormal T-helper 17 cell number [MP:0010218] <2>(0|1) (0|0|0)
- 1:   abnormal T-helper 17 cell differentiation [MP:0010221](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
V set domains (antibody variable domain-like)0.00002674Direct


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