Phenotypic Abnormality (PA): Mandibular osteomyelitis

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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:	Abnormality of skeletal morphology [HP:0011842] <17>	(86|89)	(90|52|33)
+ + + + + + 6:	Abnormality of head or neck [HP:0000152] <2>	(86|104)	(97|58|38)
+ + + + + 5:	Abnormality of the immune system [HP:0002715] <3>	(38|52)	(40|29|16)
+ + + + + 5:	Abnormal axial skeleton morphology [HP:0009121] <6>	(47|61)	(51|30|26)
+ + + + + 5:	Abnormality of the head [HP:0000234] <6>	(85|102)	(96|57|38)
+ + + + 4:	Abnormal skull morphology [HP:0000929] <14>	(25|38)	(28|22|20)
+ + + + 4:	Abnormality of immune system physiology [HP:0010978] <14>	(29|37)	(31|22|11)
+ + + + 4:	Phenotypic abnormality [HP:0000118] <25>
+ + + 3:	Abnormal inflammatory response [HP:0012647] <2>	(17|20)	(18|11|3)
+ + + 3:	Abnormality of facial skeleton [HP:0011821] <14>	(4|4)	(5|6|9)
+ + + 3:	Abnormality of the skeletal system [HP:0000924] <7>	(88|98)	(93|55|34)
+ + 2:	Abnormal jaw morphology [HP:0030791] <4>	(3|2)	(3|5|8)
+ + 2:	Abnormality of skeletal physiology [HP:0011843] <8>	(17|23)	(17|15|15)
+ + 2:	Increased inflammatory response [HP:0012649] <27>	(15|18)	(16|9|3)
+ 1:	Abnormality of the mandible [HP:0000277] <20>	(3|1)	(3|3|7)
+ 1:	Osteomyelitis [HP:0002754] <4>	(0|0)	(0|0|0)
0:	Mandibular osteomyelitis [HP:0007626]	(0|0)	(0|0|0)

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