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Mammalian Phenotype (MP): abnormal ocular surface 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)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ 1:   abnormal eye morphology [MP:0002092] <23>(39|49) (46|25|15)
0:   abnormal ocular surface morphology [MP:0013754] <4>(0|1) (2|0|0)
- 1:   abnormal conjunctiva morphology [MP:0001310] <7>(0|0) (0|0|0)
- 1:   abnormal lacrimal apparatus morphology [MP:0008968] <3>(0|0) (0|0|0)
- 1:   abnormal corneal epithelium morphology [MP:0006000](0|0) (1|0|0)
- 1:   abnormal tear film morphology [MP:0014131](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
TNF receptor-like0.000909Direct


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)
TNF receptor-like0.0007032Direct
Intermediate filament protein, coiled coil region0.003756Inherited


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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