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Mammalian Phenotype (MP): abnormal foregut morphology

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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:   digestive/alimentary phenotype [MP:0005381] <2>(38|46) (40|19|9)
+ + 2:   abnormal digestive system morphology [MP:0000462] <21>(30|38) (31|13|3)
+ 1:   abnormal digestive system development [MP:0003119] <9>(3|3) (3|1|0)
0:   abnormal foregut morphology [MP:0000474] <2>(1|2) (1|0|0)
- 1:   absent foregut [MP:0012083](0|0) (0|0|0)
- 1:   truncated foregut [MP:0012084](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
SMAD MH1 domain0.000000006088Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
SMAD domain0.000000004908Direct
SMAD MH1 domain0.000000004908Direct


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)
SMAD MH1 domain0.000000002303Direct


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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