Phenotypic Abnormality (PA): Episcleritis

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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 the immune system [HP:0002715] <3>	(38|52)	(40|29|16)
+ + + + 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 the eye [HP:0000478] <2>	(64|78)	(69|38|28)
+ + 2:	Abnormal eye morphology [HP:0012372] <12>	(39|48)	(41|29|22)
+ + 2:	Increased inflammatory response [HP:0012649] <27>	(15|18)	(16|9|3)
+ + 2:	Abnormal eye physiology [HP:0012373] <17>	(34|47)	(37|22|20)
+ 1:	Inflammatory abnormality of the eye [HP:0100533] <6>	(6|7)	(6|3|0)
+ 1:	Abnormal sclera morphology [HP:0000591] <12>	(0|1)	(1|0|0)
0:	Episcleritis [HP:0100534]	(0|0)	(0|0|0)

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