Human Phenotype Ontology 
Grandparent Node:
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Abnormality of immune serum protein physiology (HP:0011111)help
Parent Node:
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Abnormal cytokine signaling (HP:0031406)help
..Starting node
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Impaired cytokine signaling (HP:0031407)help
Term ID: 31407
Name: Impaired cytokine signaling
Synonym: Cytokine signaling defect; Cytokine signalling defect; Impaired cytokine signalling
Definition: A defect or impairment 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:0031407
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031407HP:0031407Impaired cytokine signaling0 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.