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Phenotypic Abnormality (PA): Spastic dysarthria

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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:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + + + + 5:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Abnormality of central motor function [HP:0011442] <10>(22|26) (30|16|7)
+ + + + 4:   Abnormal muscle physiology [HP:0011804] <12>(44|59) (51|22|5)
+ + + + 4:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + + 3:   Abnormality of higher mental function [HP:0011446] <9>(38|45) (40|24|8)
+ + + 3:   Upper motor neuron dysfunction [HP:0002493] <4>(9|15) (13|8|4)
+ + + 3:   Abnormal muscle tone [HP:0003808] <3>(23|37) (27|15|5)
+ + 2:   Neurological speech impairment [HP:0002167] <20>(5|9) (5|4|1)
+ + 2:   Hypertonia [HP:0001276] <3>(4|9) (5|5|2)
+ 1:   Spasticity [HP:0001257] <13>(3|6) (3|3|2)
+ 1:   Dysarthria [HP:0001260] <3>(2|5) (2|1|0)
0:   Spastic dysarthria [HP:0002464](0|0) (0|0|0)