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Mammalian Phenotype (MP): abnormal gastrointestinal motility

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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>
+ + 2:   digestive/alimentary phenotype [MP:0005381] <2>(38|46) (40|19|9)
+ 1:   abnormal digestive system physiology [MP:0001663] <18>(16|16) (17|7|5)
0:   abnormal gastrointestinal motility [MP:0011082] <5>(1|0) (1|0|0)
- 1:   abnormal intestinal peristalsis [MP:0003289] <2>(0|0) (0|0|0)
- 1:   abnormal intestinal transit time [MP:0006001] <2>(0|0) (0|0|0)
- 1:   abnormal esophageal peristalsis [MP:0004108] <1>(0|0) (0|0|0)
- 1:   intestinal obstruction [MP:0003270] <1>(0|0) (0|0|0)
- 1:   impaired gastric peristalsis [MP:0009854](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-like0.0005729Direct


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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)
Family A G protein-coupled receptor-like0.0003038Direct


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