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Mammalian Phenotype (MP): abnormal retinal development

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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:   abnormal posterior eye segment morphology [MP:0005195] <4>(21|24) (23|14|8)
+ + + 3:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ + 2:   abnormal eye morphology [MP:0002092] <23>(39|49) (46|25|15)
+ + 2:   abnormal ocular fundus morphology [MP:0002864] <2>(19|23) (21|14|8)
+ 1:   abnormal retina morphology [MP:0001325] <23>(19|23) (21|14|8)
+ 1:   abnormal eye development [MP:0001286] <22>(6|5) (6|2|2)
0:   abnormal retinal development [MP:0009772] <1>(1|0) (1|0|1)
- 1:   abnormal retinal progenitor cell morphology [MP:0006071](1|0) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Toll/Interleukin receptor TIR domain0.00003767Direct


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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)
Toll/Interleukin receptor TIR domain0.00001745Direct

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.0006309Direct


    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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