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Phenotypic Abnormality (PA): Scleral schwannoma

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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 the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Neoplasm of the nervous system [HP:0004375] <2>(3|6) (3|2|0)
+ + + 3:   Neoplasm [HP:0002664] <2>(20|21) (23|8|3)
+ + + 3:   Abnormality of the eye [HP:0000478] <2>(64|78) (69|38|28)
+ + + 3:   Abnormal peripheral nervous system morphology [HP:0000759] <14>(14|17) (18|6|0)
+ + 2:   Neoplasm by anatomical site [HP:0011793] <24>(18|19) (20|7|2)
+ + 2:   Neoplasm of the peripheral nervous system [HP:0100007] <6>(0|0) (0|0|0)
+ + 2:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
+ 1:   Neoplasm of the eye [HP:0100012] <5>(0|0) (0|0|0)
+ 1:   Abnormal sclera morphology [HP:0000591] <12>(0|1) (1|0|0)
+ 1:   Schwannoma [HP:0100008] <3>(0|0) (0|0|0)
0:   Scleral schwannoma [HP:0100011](0|0) (0|0|0)