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Phenotypic Abnormality (PA): Jaw hyporeflexia

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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>(87|107) (98|59|37)
+ + + + + + 6:   Abnormality of the nervous system [HP:0000707] <4>(147|170) (164|102|45)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the head [HP:0000234] <6>(86|105) (97|58|37)
+ + + + + 5:   Abnormality of nervous system physiology [HP:0012638] <26>(104|120) (119|81|38)
+ + + + 4:   Abnormality of movement [HP:0100022] <19>(26|25) (28|13|2)
+ + + + 4:   Abnormality of the face [HP:0000271] <14>(72|88) (83|47|30)
+ + + + 4:   Abnormality of the musculature [HP:0003011] <3>(62|74) (69|31|7)
+ + + 3:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|34) (32|13|3)
+ + + 3:   Abnormal reflex [HP:0031826] <5>(8|8) (8|6|1)
+ + + 3:   Abnormality of facial soft tissue [HP:0011799] <7>(4|3) (4|3|0)
+ + 2:   Abnormality of facial musculature [HP:0000301] <12>(4|3) (4|3|0)
+ + 2:   Reduced tendon reflexes [HP:0001315] <2>(4|3) (4|3|0)
+ 1:   Abnormality of jaw muscles [HP:0045037] <2>(2|2) (2|1|0)
+ 1:   Hyporeflexia [HP:0001265] <3>(2|0) (2|2|0)
0:   Jaw hyporeflexia [HP:0012392](0|0) (0|0|0)