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Mammalian Phenotype (MP): retinal degeneration

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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:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ + + + 4:   abnormal eye morphology [MP:0002092] <23>(39|49) (46|25|15)
+ + + 3:   abnormal posterior eye segment morphology [MP:0005195] <4>(21|24) (23|14|8)
+ + 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)
0:   retinal degeneration [MP:0001326] <1>(2|1) (2|0|0)
- 1:   retinal macular degeneration [MP:0020038](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
GroEL equatorial domain-like0.000004781Direct
Clc chloride channel0.00004865Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Clc chloride channel0.0000251Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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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)
GroEL equatorial domain-like0.000002044Direct
Clc chloride channel0.00002288Direct


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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