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Phenotypic Abnormality (PA): Iris melanoma

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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:   Neoplasm [HP:0002664] <2>(20|21) (23|8|3)
+ + + + 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:   Neoplasm by histology [HP:0011792] <7>(5|7) (6|3|0)
+ + + 3:   Neoplasm by anatomical site [HP:0011793] <24>(18|19) (20|7|2)
+ + 2:   Melanoma [HP:0002861] <2>(1|1) (1|0|0)
+ + 2:   Abnormal uvea morphology [HP:0000553] <5>(7|8) (8|5|7)
+ + 2:   Neoplasm of the eye [HP:0100012] <5>(0|0) (0|0|0)
+ + 2:   Abnormal anterior eye segment morphology [HP:0004328] <8>(17|22) (19|15|14)
+ 1:   Uveal melanoma [HP:0007716] <3>(0|0) (0|0|0)
+ 1:   Abnormality iris morphology [HP:0000525] <14>(2|4) (3|2|0)
0:   Iris melanoma [HP:0011524](0|0) (0|0|0)