Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of immune system physiology (HP:0010978)help
Parent Node:
expandAbnormality of immune serum protein physiology (HP:0011111)help
..Starting node
..expandAbnormal cytokine signaling (HP:0031406)help
Term ID: 31406
Name: Abnormal cytokine signaling
Synonym: Abnormal cytokine signalling
Definition: Any abnormality in the series of molecular signals initiated by the binding of a cytokine to a receptor on the surface of a cell, and ending with regulation of a downstream cellular process, e.g. transcription.
Comments:
Reference: HP:0031406
Genes and Diseases:
 
       Child Nodes:
........expandImpaired cytokine signaling (HP:0031407) help

 Sister Nodes: 
..expandAbnormality of cytokine secretion (HP:0011113) help
..expandAbnormality of serum cytokine level (HP:0011112) 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:0031406HP:0031406Abnormal cytokine signaling0 CL E G H
HP:0031406HP:0031407Impaired cytokine signaling1 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.