Phenotypic Abnormality (PA): Pancreatitis

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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 immune system [HP:0002715] <3>	(38|52)	(40|29|16)
+ + + + 4:	Abnormality of the digestive system [HP:0025031] <6>	(67|77)	(77|47|25)
+ + + 3:	Abnormality of the abdominal organs [HP:0002012] <6>	(27|27)	(30|14|4)
+ + + 3:	Abnormality of immune system physiology [HP:0010978] <14>	(29|37)	(31|22|11)
+ + 2:	Abnormal inflammatory response [HP:0012647] <2>	(17|20)	(18|11|3)
+ + 2:	Abnormality of the pancreas [HP:0001732] <3>	(6|5)	(7|3|0)
+ 1:	Increased inflammatory response [HP:0012649] <27>	(15|18)	(16|9|3)
+ 1:	Abnormality of pancreas physiology [HP:0012091] <3>	(1|2)	(1|1|0)
0:	Pancreatitis [HP:0001733] <4>	(0|0)	(0|0|0)
- 1:	Acute pancreatitis [HP:0001735]	(0|0)	(0|0|0)
- 1:	Chronic calcifying pancreatitis [HP:0005236]	(0|0)	(0|0|0)
- 1:	Chronic pancreatitis [HP:0006280]	(0|0)	(0|0|0)
- 1:	Recurrent pancreatitis [HP:0100027]	(0|0)	(0|0|0)

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