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Mammalian Phenotype (MP): absent lymphocyte

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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)
+ + + + + + + + + 9:   mammalian phenotype [MP:0000001] <29>
+ + + + + + + 7:   immune system phenotype [MP:0005387] <2>(76|114) (86|66|35)
+ + + + + + + 7:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + + + + + 6:   abnormal immune system morphology [MP:0000685] <3>(51|76) (60|35|18)
+ + + + + + 6:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(58|86) (66|47|21)
+ + + + + 5:   abnormal immune system cell morphology [MP:0000716] <5>(38|63) (48|29|16)
+ + + + + 5:   abnormal hematopoietic cell morphology [MP:0013656] <9>(49|77) (60|43|18)
+ + + + 4:   abnormal mononuclear cell morphology [MP:0008247] <2>(34|57) (41|28|14)
+ + + + 4:   abnormal leukocyte morphology [MP:0008246] <4>(37|62) (47|29|15)
+ + + + 4:   abnormal hematopoietic cell number [MP:0011180] <7>(34|57) (43|29|13)
+ + + 3:   decreased hematopoietic cell number [MP:0011182] <5>(21|34) (27|21|11)
+ + + 3:   abnormal leukocyte cell number [MP:0000217] <8>(29|49) (37|25|12)
+ + + 3:   abnormal lymphocyte morphology [MP:0002619] <5>(28|46) (33|26|14)
+ + 2:   abnormal lymphocyte cell number [MP:0000717] <6>(18|38) (25|21|9)
+ + 2:   decreased leukocyte cell number [MP:0000221] <5>(17|28) (24|18|10)
+ 1:   decreased lymphocyte cell number [MP:0005016] <5>(16|28) (22|16|7)
0:   absent lymphocyte [MP:0000726] <3>(0|1) (0|0|0)
- 1:   absent T cells [MP:0008070] <4>(0|0) (0|0|0)
- 1:   absent B cells [MP:0008071] <2>(0|1) (0|0|0)
- 1:   absent NK cells [MP:0008046] <1>(0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Interferon regulatory factor 3 (IRF3), transactivation domain0.00001935Direct


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