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Phenotypic Abnormality (PA): Abnormality of central sensory function

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ 1:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
0:   Abnormality of central sensory function [HP:0011730] <4>(0|0) (0|0|0)
- 1:   Agraphesthesia [HP:0011812](0|0) (0|0|0)
- 1:   Astereognosia [HP:0010527](0|0) (0|0|0)
- 1:   Impaired touch localization [HP:0011811](0|0) (0|0|0)
- 1:   Impaired two-point discrimination [HP:0011810](0|0) (0|0|0)