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Phenotypic Abnormality (PA): Retinal degeneration

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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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the eye [HP:0000478] <2>(64|78) (69|38|28)
+ + + + 4:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
+ + + 3:   Abnormal posterior eye segment morphology [HP:0004329] <3>(16|11) (17|6|8)
+ + 2:   Abnormal fundus morphology [HP:0001098] <10>(15|11) (16|6|8)
+ 1:   Abnormal retinal morphology [HP:0000479] <27>(11|6) (12|5|8)
0:   Retinal degeneration [HP:0000546] <4>(1|0) (1|0|1)
- 1:   Peripheral retinal degeneration [HP:0007769] <4>(0|0) (0|0|0)
- 1:   Retinal atrophy [HP:0001105] <4>(0|0) (0|0|0)
- 1:   Macular degeneration [HP:0000608] <3>(0|0) (0|0|1)
- 1:   Retinitis pigmentosa inversa [HP:0008035](0|0) (0|0|0)


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

Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Voltage-gated potassium channels0.0009623Direct


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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)
Voltage-gated potassium channels0.0005096Direct

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57535,57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.004556Inherited


    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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