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Mammalian Phenotype (MP): abnormal astrocyte physiology

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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:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + 2:   abnormal nervous system physiology [MP:0003633] <38>(43|60) (52|31|18)
+ 1:   abnormal glial cell physiology [MP:0003690] <5>(2|2) (3|0|0)
0:   abnormal astrocyte physiology [MP:0008916] <1>(0|0) (1|0|0)
- 1:   abnormal astrocyte apoptosis [MP:0010204](0|0) (0|0|0)


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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
GTPase activation domain, GAP0.0006798Direct


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