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Phenotypic Abnormality (PA): Facial paralysis

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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)
+ + + + + + 6:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + 4:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + + + 4:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + + + 4:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + + 3:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + + 3:   Abnormal peripheral nervous system morphology [HP:0000759] <14>(14|17) (18|6|0)
+ + + 3:   Abnormality of facial soft tissue [HP:0011799] <7>(2|3) (4|3|0)
+ + + 3:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
+ + 2:   Abnormal cranial nerve morphology [HP:0001291] <10>(2|1) (2|1|0)
+ + 2:   Abnormality of facial musculature [HP:0000301] <12>(2|3) (4|3|0)
+ + 2:   Abnormality of central motor function [HP:0011442] <10>(22|26) (30|16|7)
+ 1:   Weakness of facial musculature [HP:0030319] <3>(0|1) (1|1|0)
+ 1:   Paralysis [HP:0003470] <6>(4|3) (4|0|0)
+ 1:   Cranial nerve compression [HP:0001293] <3>(0|0) (0|0|0)
0:   Facial paralysis [HP:0007209](0|0) (0|0|0)