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Mammalian Phenotype (MP): abnormal retinal pigment epithelium 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)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   abnormal posterior eye segment morphology [MP:0005195] <4>(21|24) (23|14|8)
+ + + 3:   pigmentation phenotype [MP:0001186] <13>(4|5) (6|1|3)
+ + + 3:   abnormal ocular fundus morphology [MP:0002864] <2>(19|23) (21|14|8)
+ + + 3:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ + 2:   abnormal retina morphology [MP:0001325] <23>(19|23) (21|14|8)
+ + 2:   abnormal eye morphology [MP:0002092] <23>(39|49) (46|25|15)
+ + 2:   abnormal extracutaneous pigmentation [MP:0009389] <4>(1|1) (2|0|1)
+ 1:   abnormal retinal layer morphology [MP:0003727] <3>(11|16) (12|8|6)
+ 1:   abnormal eye pigmentation [MP:0001324] <8>(1|1) (2|0|1)
0:   abnormal retinal pigment epithelium morphology [MP:0005201] <3>(0|1) (1|0|1)
- 1:   abnormal retinal pigmentation [MP:0005103] <1>(0|0) (0|0|0)
- 1:   retinal pigment epithelium atrophy [MP:0005548](0|0) (0|0|0)
- 1:   retinal pigment epithelium hyperplasia [MP:0005549](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
YWTD domain0.0008689Direct


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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)
YWTD domain0.0007156Direct

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57424,57424,57424
  • 57424 - LDL receptor-like module
  • 57424 - LDL receptor-like module
  • 57424 - LDL receptor-like module
  • 0.0009126Direct


    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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