Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of neutrophils (HP:0001874)help
Parent Node:
expandAbnormality of neutrophil morphology (HP:0011992)help
..Starting node
..expandNeutrophil inclusion bodies (HP:0008264)help
Term ID: 8264
Name: Neutrophil inclusion bodies
Synonym:
Definition: The presence of intracellular inclusion bodies (aggregates of stainable substances, usually proteins) in neutrophils. Cytoplasmic neutrophil inclusions (oval, basophilic) are also known as Doehle bodies.
Comments:
Reference: HP:0008264
Genes and Diseases:
 
       Child Nodes:
........expandLeukocyte inclusion bodies (HP:0040235) help

 Sister Nodes: 
..expandAbsent neutrophil specific granules (HP:0012551) help
..expandHypersegmentation of neutrophil nuclei (HP:0004821) help
..expandHyposegmentation of neutrophil nuclei (HP:0011447) help
..expandIncreased neutrophil nuclear projections (HP:0012552) help
..expandPyknotic bone marrow neutrophils (HP:0031019) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008264HP:0008264Neutrophil inclusion bodies0MYH9 CL E G H46277579OMIM:155100Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss.297
HP:0008264HP:0008264Neutrophil inclusion bodies0MYH9 CL E G H46277579ORPHA:182050MYH9-related diseaseHP:0040282 - Frequent297
HP:0008264HP:0040235Leukocyte inclusion bodies1MYH9 CL E G H46277579OMIM:155100Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss.297


Genes (1) :MYH9

Diseases (2) :OMIM:155100 ORPHA:182050
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.