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Phenotypic Abnormality (PA): Bulbar palsy

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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:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormal muscle physiology [HP:0011804] <12>(44|59) (51|22|5)
+ + 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)
+ 1:   Muscle weakness [HP:0001324] <22>(13|14) (15|4|0)
0:   Bulbar palsy [HP:0001283](0|0) (0|0|0)