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Phenotypic Abnormality (PA): Iris hypopigmentation

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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 uvea morphology [HP:0000553] <5>(7|8) (8|5|7)
+ + + 3:   Abnormal anterior eye segment morphology [HP:0004328] <8>(17|21) (19|15|14)
+ + 2:   Abnormality iris morphology [HP:0000525] <14>(2|4) (3|2|0)
+ 1:   Abnormal iris pigmentation [HP:0008034] <7>(0|1) (1|1|0)
0:   Iris hypopigmentation [HP:0007730] <1>(0|1) (0|1|0)
- 1:   Ocular albinism [HP:0001107](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
PDZ domain0.0007213Direct


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Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
50156,50156
  • 50156 - PDZ domain-like
  • 50156 - PDZ domain-like
  • 0.00004342Direct