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Phenotypic Abnormality (PA): Retinal detachment

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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 detachment [HP:0000541] <5>(1|1) (2|0|0)
- 1:   Tractional retinal detachment [HP:0007917] <1>(0|0) (0|0|0)
- 1:   Exudative retinal detachment [HP:0012231](0|0) (0|0|0)
- 1:   Peripheral retinal detachment [HP:0007929](0|0) (0|0|0)
- 1:   Retinal nonattachment [HP:0007899](0|0) (0|0|0)
- 1:   Rhegmatogenous retinal detachment [HP:0012230](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
FnI-like domain0.0006029Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
VWC domain0.000001171Direct


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)
FnI-like domain0.0003093Direct
Nucleotide-diphospho-sugar transferases0.0007623Direct


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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