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Mammalian Phenotype (MP): renal glomerulus fibrosis

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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)
+ + + + + 5:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   renal/urinary system phenotype [MP:0005367] <2>(41|47) (46|26|11)
+ + + 3:   abnormal renal/urinary system morphology [MP:0000516] <14>(31|36) (36|22|11)
+ + + 3:   abnormal kidney cortex morphology [MP:0000521] <9>(10|16) (12|9|3)
+ + + 3:   abnormal nephron morphology [MP:0003881] <8>(19|22) (21|12|3)
+ + 2:   abnormal kidney morphology [MP:0002135] <29>(26|28) (28|15|6)
+ + 2:   abnormal renal corpuscle morphology [MP:0002827] <6>(10|15) (12|9|3)
+ 1:   renal fibrosis [MP:0003985] <2>(0|0) (2|0|0)
+ 1:   abnormal renal glomerulus morphology [MP:0005325] <13>(9|14) (12|7|2)
0:   renal glomerulus fibrosis [MP:0011377](0|0) (1|0|0)


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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
C-type lectin-like0.0007757Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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