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Phenotypic Abnormality (PA): Retrocollis

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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 movement [HP:0100022] <19>(23|25) (25|14|3)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Dystonia [HP:0001332] <8>(1|2) (1|1|0)
+ + + + 4:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + 4:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + + 3:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
+ + + 3:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + + 3:   Focal dystonia [HP:0004373] <3>(1|2) (1|1|0)
+ + + 3:   Abnormality of the neck [HP:0000464] <15>(4|5) (5|2|1)
+ + 2:   Abnormal morphology of the musculature of the neck [HP:0011006] <5>(1|1) (1|1|0)
+ + 2:   Abnormality of central motor function [HP:0011442] <10>(22|26) (30|16|7)
+ + 2:   Craniofacial dystonia [HP:0012179] <5>(1|1) (1|1|0)
+ 1:   Torticollis [HP:0000473] <1>(1|1) (1|1|0)
0:   Retrocollis [HP:0002544](0|0) (0|0|0)