Phenotypic Abnormality (PA): Aplasia of the parotid gland

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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)
+ + + + + + + + + 9:	Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + + 8:	Abnormality of head or neck [HP:0000152] <2>	(86|104)	(97|58|38)
+ + + + + + + 7:	Abnormality of the head [HP:0000234] <6>	(85|102)	(96|57|38)
+ + + + + + 6:	Abnormality of the face [HP:0000271] <14>	(70|85)	(82|46|31)
+ + + + + 5:	Abnormality of the mouth [HP:0000153] <2>	(37|57)	(46|32|22)
+ + + + 4:	Abnormal oral morphology [HP:0031816] <6>	(35|53)	(44|30|21)
+ + + 3:	Abnormal oral cavity morphology [HP:0000163] <14>	(28|43)	(36|21|15)
+ + 2:	Abnormal salivary gland morphology [HP:0010286] <6>	(1|0)	(1|1|1)
+ 1:	Abnormal parotid gland morphology [HP:0000197] <4>	(1|0)	(1|1|1)
0:	Aplasia of the parotid gland [HP:0009740]	(0|0)	(0|0|0)

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