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Phenotypic Abnormality (PA): Retinal neoplasm

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormal posterior eye segment morphology [HP:0004329] <3>(16|11) (17|6|8)
+ + + 3:   Abnormality of the eye [HP:0000478] <2>(64|78) (69|38|28)
+ + + 3:   Neoplasm [HP:0002664] <2>(20|21) (23|8|3)
+ + 2:   Abnormal fundus morphology [HP:0001098] <10>(15|11) (16|6|8)
+ + 2:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
+ + 2:   Neoplasm by anatomical site [HP:0011793] <24>(18|19) (20|7|2)
+ 1:   Neoplasm of the eye [HP:0100012] <5>(0|0) (0|0|0)
+ 1:   Abnormal retinal morphology [HP:0000479] <27>(11|6) (12|5|8)
0:   Retinal neoplasm [HP:0012777] <1>(0|0) (0|0|0)
- 1:   Retinoblastoma [HP:0009919](0|0) (0|0|0)