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Phenotypic Abnormality (PA): Lymphopenia

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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)
+ + + + + + 6:   Abnormality of the immune system [HP:0002715] <3>(38|52) (40|29|16)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormal immune system morphology [HP:0032251] <3>(11|11) (11|6|2)
+ + + + 4:   Abnormal cellular immune system morphology [HP:0010987] <1>(10|10) (10|6|2)
+ + + + 4:   Abnormality of blood and blood-forming tissues [HP:0001871] <11>(24|35) (31|16|5)
+ + + 3:   Abnormal leukocyte morphology [HP:0001881] <4>(8|9) (9|5|2)
+ + 2:   Abnormal leukocyte count [HP:0011893] <7>(4|8) (6|5|2)
+ + 2:   Abnormal lymphocyte morphology [HP:0004332] <8>(2|2) (2|0|0)
+ 1:   Abnormal lymphocyte count [HP:0040088] <4>(0|1) (0|0|0)
+ 1:   Leukopenia [HP:0001882] <1>(3|5) (3|3|2)
0:   Lymphopenia [HP:0001888] <2>(0|1) (0|0|0)
- 1:   Decrease in T cell count [HP:0005403] <4>(0|0) (0|0|0)
- 1:   B lymphocytopenia [HP:0010976] <2>(0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Nitrogenase iron protein-like0.0001227Direct


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