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Phenotypic Abnormality (PA): Hamartoma of the eye

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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:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + 3:   Abnormality of the eye [HP:0000478] <2>(64|78) (69|38|28)
+ + + 3:   Neoplasm [HP:0002664] <2>(20|21) (23|8|3)
+ + + 3:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + 2:   Neoplasm by anatomical site [HP:0011793] <24>(18|19) (20|7|2)
+ + 2:   Abnormality of the orbital region [HP:0000315] <4>(17|24) (19|5|4)
+ + 2:   Neoplasm by histology [HP:0011792] <7>(5|7) (6|3|0)
+ + 2:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
+ 1:   Hamartoma of the orbital region [HP:0030670] <2>(0|0) (0|0|0)
+ 1:   Hamartoma [HP:0010566] <10>(0|0) (0|0|0)
+ 1:   Neoplasm of the eye [HP:0100012] <5>(0|0) (0|0|0)
0:   Hamartoma of the eye [HP:0010568] <3>(0|0) (0|0|0)
- 1:   Retinal hamartoma [HP:0009594] <5>(0|0) (0|0|0)
- 1:   Conjunctival hamartoma [HP:0100780](0|0) (0|0|0)
- 1:   Lisch nodules [HP:0009737](0|0) (0|0|0)