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Phenotypic Abnormality (PA): Abnormal granulocytopoietic cell morphology

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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 blood and blood-forming tissues [HP:0001871] <11>(24|35) (31|16|5)
+ 1:   Abnormality of bone marrow cell morphology [HP:0005561] <5>(3|4) (3|1|0)
0:   Abnormal granulocytopoietic cell morphology [HP:0012135] <3>(0|0) (0|0|0)
- 1:   Abnormal number of granulocyte precursors [HP:0012137] <2>(0|0) (0|0|0)
- 1:   Dysplastic granulopoesis [HP:0012136](0|0) (0|0|0)
- 1:   Myelokathexis [HP:0031160](0|0) (0|0|0)