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Phenotypic Abnormality (PA): Immunologic hypersensitivity

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the immune system [HP:0002715] <3>(38|52) (40|29|16)
+ 1:   Abnormality of immune system physiology [HP:0010978] <14>(29|37) (31|22|11)
0:   Immunologic hypersensitivity [HP:0100326] <6>(0|0) (0|0|0)
- 1:   Allergy [HP:0012393] <16>(0|0) (0|0|0)
- 1:   Anaphylactic shock [HP:0100845] <5>(0|0) (0|0|0)
- 1:   Asthma [HP:0002099] <3>(0|0) (0|0|0)
- 1:   Airborn particle hypersensitivity [HP:0032439](0|0) (0|0|0)
- 1:   Celiac disease [HP:0002608](0|0) (0|0|0)
- 1:   Immediate-type hypersensitivity drug reaction [HP:0032378](0|0) (0|0|0)