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Phenotypic Abnormality (PA): Abnormal pupil morphology

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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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the eye [HP:0000478] <2>(64|78) (69|38|28)
+ + + 3:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
+ + 2:   Abnormal anterior eye segment morphology [HP:0004328] <8>(17|21) (19|15|14)
+ + 2:   Abnormal uvea morphology [HP:0000553] <5>(7|8) (8|5|7)
+ 1:   Abnormality iris morphology [HP:0000525] <14>(2|4) (3|2|0)
0:   Abnormal pupil morphology [HP:0000615] <7>(0|1) (0|0|0)
- 1:   Abnormal pupil shape [HP:0025309] <1>(0|0) (0|0|0)
- 1:   Anisocoria [HP:0009916](0|0) (0|0|0)
- 1:   Ectopia pupillae [HP:0009918](0|0) (0|0|0)
- 1:   Leukocoria [HP:0000555](0|0) (0|0|0)
- 1:   Microcoria [HP:0025492](0|0) (0|0|0)
- 1:   Persistent pupillary membrane [HP:0009917](0|0) (0|0|0)
- 1:   Polycoria [HP:0011500](0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
BCR-homology GTPase activation domain (BH-domain)0.0001552Direct


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