Phenotypic Abnormality (PA): Recurrent otitis media

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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:	Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:	Abnormality of the ear [HP:0000598] <2>	(17|32)	(21|13|11)
+ + + + 4:	Abnormality of the immune system [HP:0002715] <3>	(38|52)	(40|29|16)
+ + + 3:	Abnormal ear morphology [HP:0031703] <5>	(15|26)	(18|11|10)
+ + + 3:	Abnormality of immune system physiology [HP:0010978] <14>	(29|37)	(31|22|11)
+ + + 3:	Abnormal inflammatory response [HP:0012647] <2>	(17|20)	(18|11|3)
+ + 2:	Abnormality of the middle ear [HP:0000370] <10>	(1|5)	(1|1|5)
+ + 2:	Unusual infection [HP:0032101] <11>	(15|19)	(17|6|0)
+ + 2:	Increased inflammatory response [HP:0012649] <27>	(15|18)	(16|9|3)
+ 1:	Otitis media [HP:0000388] <4>	(0|3)	(0|1|1)
+ 1:	Recurrent infections [HP:0002719] <15>	(6|12)	(8|4|0)
0:	Recurrent otitis media [HP:0000403]	(0|0)	(0|0|0)

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