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Mammalian Phenotype (MP): abnormal spleen weight

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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)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   immune system phenotype [MP:0005387] <2>(76|114) (86|66|35)
+ + + + 4:   abnormal immune system morphology [MP:0000685] <3>(51|76) (60|35|18)
+ + + + 4:   hematopoietic system phenotype [MP:0005397] <2>(72|102) (78|63|30)
+ + + 3:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(58|86) (66|47|21)
+ + + 3:   abnormal immune system organ morphology [MP:0002722] <8>(21|31) (26|15|9)
+ + 2:   abnormal spleen morphology [MP:0000689] <16>(10|15) (12|8|8)
+ + 2:   abnormal lymph organ size [MP:0002221] <5>(7|16) (10|10|5)
+ 1:   abnormal spleen size [MP:0002224] <3>(2|7) (5|4|4)
0:   abnormal spleen weight [MP:0004951] <2>(0|1) (0|0|0)
- 1:   decreased spleen weight [MP:0004953](0|0) (0|0|0)
- 1:   increased spleen weight [MP:0004952](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Hypoxia-inducible factor Hif2a, C-terminal domain0.0003618Direct


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