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Phenotypic Abnormality (PA): Buphthalmos

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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)
+ + + 3:   Abnormal anterior eye segment morphology [HP:0004328] <8>(17|21) (19|15|14)
+ + + 3:   Abnormal eye physiology [HP:0012373] <17>(34|47) (37|22|20)
+ + 2:   Ocular anterior segment dysgenesis [HP:0007700] <7>(1|2) (1|0|0)
+ + 2:   Abnormality of globe size [HP:0100887] <3>(3|2) (3|1|0)
+ + 2:   Glaucoma [HP:0000501] <4>(1|1) (1|0|0)
+ 1:   Abnormally large globe [HP:0001090] <2>(0|0) (0|0|0)
+ 1:   Developmental glaucoma [HP:0001087] <3>(0|0) (0|0|0)
0:   Buphthalmos [HP:0000557](0|0) (0|0|0)