SUPERFAMILY 1.75 HMM library and genome assignments server

SUPERFAMILY 2 can be accessed from supfam.org. Please contact us if you experience any problems.

Phenotypic Abnormality (PA): Juxtafoveal choroidal neovascularization

(show info)

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

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