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Phenotypic Abnormality (PA): Hypoplasia of facial musculature

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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)
+ + + + + 5:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + 4:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + + 3:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + 2:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
+ + 2:   Abnormality of facial soft tissue [HP:0011799] <7>(2|3) (4|3|0)
+ 1:   Abnormality of facial musculature [HP:0000301] <12>(2|3) (4|3|0)
0:   Hypoplasia of facial musculature [HP:0004660](0|0) (0|0|0)