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Phenotypic Abnormality (PA): Choroidal neovascularization

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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 posterior eye segment morphology [HP:0004329] <3>(16|11) (17|6|8)
+ + + + 4:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
+ + + 3:   Abnormal uvea morphology [HP:0000553] <5>(7|8) (8|5|7)
+ + + 3:   Abnormal fundus morphology [HP:0001098] <10>(15|11) (16|6|8)
+ + 2:   Abnormal choroid morphology [HP:0000610] <6>(3|1) (4|1|2)
+ + 2:   Abnormal retinal morphology [HP:0000479] <27>(11|6) (12|5|8)
+ 1:   Abnormal macular morphology [HP:0001103] <14>(2|0) (1|0|1)
+ 1:   Abnormal morphology of the choroidal vasculature [HP:0025568] <5>(1|0) (1|0|0)
0:   Choroidal neovascularization [HP:0011506] <3>(1|0) (1|0|0)
- 1:   Extrafoveal choroidal neovascularization [HP:0031239](0|0) (0|0|0)
- 1:   Juxtafoveal choroidal neovascularization [HP:0031240](0|0) (0|0|0)
- 1:   Subfoveal choroidal neovascularization [HP:0031241](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)
Growth factor receptor domain0.0009099Direct


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)
Growth factor receptor domain0.0004801Direct


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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