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Phenotypic Abnormality (PA): Macular 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)
+ + + + + + + 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:   Abnormal macular morphology [HP:0001103] <14>(2|0) (1|0|1)
+ 1:   Retinal degeneration [HP:0000546] <4>(1|0) (1|0|1)
0:   Macular degeneration [HP:0000608] <3>(0|0) (0|0|1)
- 1:   Macular atrophy [HP:0007401] <1>(0|0) (0|0|0)
- 1:   Cystoid macular degeneration [HP:0008028](0|0) (0|0|0)
- 1:   Foveal degeneration [HP:0025146](0|0) (0|0|0)


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Supra-domain (including individual superfamily)

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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
  • 0.0001882Direct