Phenotypic Abnormality (PA): Reduced antigen-specific T cell proliferation

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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:	Abnormal cellular phenotype [HP:0025354] <3>	(10|10)	(13|3|0)
+ + + + + 5:	Abnormality of metabolism/homeostasis [HP:0001939] <16>	(75|82)	(79|40|16)
+ + + + 4:	Abnormal cellular physiology [HP:0011017] <16>	(10|10)	(13|3|0)
+ + + + 4:	Phenotypic abnormality [HP:0000118] <25>
+ + + 3:	Abnormality of the immune system [HP:0002715] <3>	(38|52)	(40|29|16)
+ + + 3:	Abnormal cell proliferation [HP:0031377] <1>	(0|0)	(0|0|0)
+ + + 3:	Abnormal lymphocyte physiology [HP:0031409] <5>	(5|6)	(5|2|0)
+ + 2:	Abnormal lymphocyte proliferation [HP:0031378] <3>	(0|0)	(0|0|0)
+ + 2:	Abnormality of immune system physiology [HP:0010978] <14>	(29|37)	(31|22|11)
+ + 2:	Abnormality of T cell physiology [HP:0011840] <6>	(0|0)	(0|0|0)
+ 1:	Impaired antigen-specific response [HP:0031404] <3>	(0|0)	(0|0|0)
+ 1:	Abnormal T cell proliferation [HP:0031379] <2>	(0|0)	(0|0|0)
0:	Reduced antigen-specific T cell proliferation [HP:0031402]	(0|0)	(0|0|0)

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