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Mammalian Phenotype (MP): abnormal intestinal absorption

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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 physiology [MP:0001663] <18>(16|16) (17|7|5)
+ 1:   abnormal digestion [MP:0001664] <4>(2|1) (2|0|0)
0:   abnormal intestinal absorption [MP:0001666] <5>(1|1) (1|0|0)
- 1:   abnormal intestinal glucose absorption [MP:0001669] <2>(0|0) (0|0|0)
- 1:   abnormal intestinal lipid absorption [MP:0005342] <2>(0|1) (0|0|0)
- 1:   abnormal intestinal mineral absorption [MP:0001670] <1>(0|0) (0|0|0)
- 1:   abnormal intestinal fructose absorption [MP:0001668](0|0) (0|0|0)
- 1:   abnormal vitamin absorption [MP:0001671](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
MFS general substrate transporter0.0001467Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
ABC transporter ATPase domain-like0.0002622Direct


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)
MFS general substrate transporter0.00007313Direct


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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