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Mammalian Phenotype (MP): abnormal blood-brain barrier function

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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)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + 2:   abnormal cardiovascular system physiology [MP:0001544] <24>(39|45) (46|26|17)
+ + 2:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ 1:   abnormal nervous system physiology [MP:0003633] <38>(43|60) (52|31|18)
+ 1:   abnormal blood vessel physiology [MP:0000249] <11>(13|17) (15|5|3)
0:   abnormal blood-brain barrier function [MP:0005167](2|0) (2|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Ferredoxin reductase-like, C-terminal NADP-linked domain0.00003653Direct
Riboflavin synthase domain-like0.00003653Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Riboflavin synthase domain-like0.00001688Direct
Ferredoxin reductase-like, C-terminal NADP-linked domain0.00001688Direct


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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