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 immune serum protein physiology (HP:0011111)

Parent Node:
Abnormality of cytokine secretion (HP:0011113)

..Starting node
..Abnormality of chemokine secretion (HP:0011115)

Term ID:

11115

Name:

Abnormality of chemokine secretion

Synonym:

Definition:

An abnormality in the production or cellular release of a chemokine (a class of cytokines).

Comments:

Reference:

HP:0011115

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormality of interferon secretion (HP:0011116)

Abnormality of interleukin secretion (HP:0011117)

Abnormality of tumor necrosis factor secretion (HP:0011118)

Defective production of NFKB1-dependent cytokines (HP:0011114)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011115	HP:0011115	Abnormality of chemokine secretion	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.