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 neutrophil physiology (HP:0011990)

Parent Node:
Impaired neutrophil bactericidal activity (HP:0011993)

..Starting node
..Impaired neutrophil killing of staphylococci (HP:0005512)

Term ID:

5512

Name:

Impaired neutrophil killing of staphylococci

Synonym:

Definition:

A reduction in the ability of neutrophils to kill the gram-positive bacteria, staphylococcus, which is commonly known as staph.

Comments:

Reference:

HP:0005512

Genes and Diseases:

Child Nodes:

Sister Nodes:

Impaired oxidative burst (HP:0003203)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005512	HP:0005512	Impaired neutrophil killing of staphylococci	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.