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Mammalian Phenotype (MP): abnormal muscle glycogen 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)
+ + + + + 5:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ + + + 4:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
+ + + 3:   abnormal glucose homeostasis [MP:0002078] <14>(15|22) (17|17|8)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   abnormal glycogen homeostasis [MP:0005438] <2>(5|3) (6|3|1)
+ + 2:   muscle phenotype [MP:0005369] <2>(49|57) (54|37|28)
+ 1:   abnormal glycogen level [MP:0005437] <5>(2|3) (3|2|1)
+ 1:   abnormal muscle morphology [MP:0002108] <16>(28|31) (31|22|21)
0:   abnormal muscle glycogen level [MP:0014068] <2>(1|0) (1|0|0)
- 1:   abnormal cardiac muscle glycogen level [MP:0014070] <2>(0|0) (0|0|0)
- 1:   abnormal skeletal muscle glycogen level [MP:0014069] <2>(1|0) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
(Trans)glycosidases0.0004017Direct


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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
(Trans)glycosidases0.0002098Direct


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