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Phenotypic Abnormality (PA): Pigmentary retinopathy

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of the eye [HP:0000478] <2>(64|78) (69|38|28)
+ + + + + 5:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
+ + + + 4:   Abnormal posterior eye segment morphology [HP:0004329] <3>(16|11) (17|6|8)
+ + + 3:   Abnormal fundus morphology [HP:0001098] <10>(15|11) (16|6|8)
+ + 2:   Abnormal retinal morphology [HP:0000479] <27>(11|6) (12|5|8)
+ 1:   Abnormality of retinal pigmentation [HP:0007703] <2>(2|2) (2|3|1)
0:   Pigmentary retinopathy [HP:0000580] <2>(1|1) (1|1|0)
- 1:   Bone spicule pigmentation of the retina [HP:0007737](0|1) (0|1|0)
- 1:   Nummular pigmentation of the fundus [HP:0030505](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
GroEL equatorial domain-like0.000117Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Laminin G-like module0.004558Inherited


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)
GroEL equatorial domain-like0.00005425Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
49899,49899
  • 49899 - Concanavalin A-like lectins/glucanases
  • 49899 - Concanavalin A-like lectins/glucanases
  • 0.003698Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
    (show help)