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Mammalian Phenotype (MP): abnormal thymus cortex 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)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   immune system phenotype [MP:0005387] <2>(76|114) (86|66|35)
+ + + + + 5:   endocrine/exocrine gland phenotype [MP:0005379] <2>(51|81) (55|36|12)
+ + + + 4:   abnormal gland morphology [MP:0002163] <8>(44|71) (50|31|11)
+ + + + 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 immune system organ morphology [MP:0002722] <8>(21|31) (26|15|9)
+ + + 3:   abnormal hematopoietic system morphology/development [MP:0002396] <5>(58|86) (66|47|21)
+ + + 3:   abnormal endocrine gland morphology [MP:0013560] <7>(16|29) (21|19|4)
+ + 2:   abnormal thymus morphology [MP:0000703] <14>(10|16) (12|10|2)
+ 1:   abnormal thymus lobule morphology [MP:0002367] <3>(4|5) (4|3|0)
0:   abnormal thymus cortex morphology [MP:0002371] <4>(0|1) (0|1|0)
- 1:   enlarged thymus cortex [MP:0013593] <1>(0|0) (0|0|0)
- 1:   small thymus cortex [MP:0013592] <1>(0|0) (0|0|0)
- 1:   absent thymus cortex [MP:0010250](0|0) (0|0|0)
- 1:   thymus cortex atrophy [MP:0013585](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
DEATH domain, DD0.0005344Direct


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Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
55550,56112
  • 55550 - SH2 domain
  • 56112 - Protein kinase-like (PK-like)
  • 0.0003642Direct