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Mammalian Phenotype (MP): decreased susceptibility to autoimmune diabetes

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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)
+ + + + + + + + 8:   mammalian phenotype [MP:0000001] <29>
+ + + + + + + 7:   immune system phenotype [MP:0005387] <2>(76|114) (86|66|35)
+ + + + + + 6:   abnormal immune system physiology [MP:0001790] <16>(59|84) (66|49|28)
+ + + + + 5:   abnormal immune tolerance [MP:0005000] <3>(11|19) (13|8|1)
+ + + + 4:   abnormal self tolerance [MP:0005005] <1>(11|19) (13|8|1)
+ + + 3:   autoimmune response [MP:0001844] <4>(11|19) (13|8|1)
+ + 2:   altered susceptibility to autoimmune disorder [MP:0002425] <2>(2|9) (3|4|1)
+ 1:   decreased susceptibility to autoimmune disorder [MP:0005351] <9>(1|7) (2|3|0)
0:   decreased susceptibility to autoimmune diabetes [MP:0004804](0|2) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
C2 set domains0.000003203Direct
Papain-like0.00001527Direct


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