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Mammalian Phenotype (MP): abnormal endolymphatic duct 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)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   hearing/vestibular/ear phenotype [MP:0005377] <2>(20|24) (23|14|5)
+ + + + 4:   abnormal ear morphology [MP:0002102] <4>(16|21) (18|14|5)
+ + + 3:   abnormal inner ear morphology [MP:0000026] <15>(13|15) (13|11|5)
+ + 2:   abnormal membranous labyrinth morphology [MP:0000035] <2>(11|14) (12|9|5)
+ 1:   abnormal vestibular labyrinth morphology [MP:0004427] <3>(1|1) (2|1|0)
0:   abnormal endolymphatic duct morphology [MP:0006011] <6>(1|1) (2|1|0)
- 1:   small endolymphatic duct [MP:0008066] <1>(1|1) (1|0|0)
- 1:   abnormal endolymphatic sac topology [MP:0013918](0|0) (0|0|0)
- 1:   absent endolymphatic duct [MP:0000041](0|0) (0|0|0)
- 1:   absent endolymphatic sac [MP:0006013](0|0) (0|0|0)
- 1:   dilated endolymphatic duct [MP:0006012](0|0) (0|0|0)
- 1:   dilated endolymphatic sac [MP:0006014](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Homeodomain-like0.00169Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Homeodomain0.006344Inherited


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)
Glucocorticoid receptor-like (DNA-binding domain)0.0007242Direct
Homeodomain-like0.0009529Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57716,57716
  • 57716 - Glucocorticoid receptor-like (DNA-binding domain)
  • 57716 - Glucocorticoid receptor-like (DNA-binding domain)
  • 0.0005091Direct


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