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Mammalian Phenotype (MP): abnormal corticosterone level

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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)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ + 2:   abnormal lipid homeostasis [MP:0002118] <9>(25|29) (29|17|10)
+ + 2:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
+ 1:   abnormal lipid level [MP:0001547] <16>(24|28) (26|16|10)
+ 1:   abnormal hormone level [MP:0003953] <15>(27|29) (30|17|8)
0:   abnormal corticosterone level [MP:0003963] <2>(1|1) (1|0|0)
- 1:   abnormal circulating corticosterone level [MP:0005345] <2>(1|1) (1|0|0)
- 1:   abnormal urine corticosterone level [MP:0011548] <2>(0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Family A G protein-coupled receptor-like0.0002045Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Rhodopsin-like0.0001006Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Family A G protein-coupled receptor-like0.0001035Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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