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Phenotypic Abnormality (PA): Coronary cataract

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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 anterior eye segment morphology [HP:0004328] <8>(17|22) (19|15|14)
+ + + 3:   Abnormality of the lens [HP:0000517] <6>(6|8) (7|9|10)
+ + 2:   Cataract [HP:0000518] <11>(3|4) (3|3|2)
+ 1:   Zonular cataract [HP:0010920] <7>(1|1) (1|0|0)
0:   Coronary cataract [HP:0025559](0|0) (0|0|0)