Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormality of neutrophils (HP:0001874)

Parent Node:
Abnormality of neutrophil morphology (HP:0011992)

..Starting node
..Increased neutrophil nuclear projections (HP:0012552)

Term ID:

12552

Name:

Increased neutrophil nuclear projections

Synonym:

Definition:

Presence of an elevated number of projections from nuclei of neutrophils. These projections can have the shape of hooks, tags, or clubs.

Comments:

Reference:

HP:0012552

Genes and Diseases:

Child Nodes:

Sister Nodes:

Absent neutrophil specific granules (HP:0012551)

Hypersegmentation of neutrophil nuclei (HP:0004821)

Hyposegmentation of neutrophil nuclei (HP:0011447)

Neutrophil inclusion bodies (HP:0008264)

Pyknotic bone marrow neutrophils (HP:0031019)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012552	HP:0012552	Increased neutrophil nuclear projections	0	CL E G H

Genes (0) :

Diseases (0) :

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