Human Phenotype Ontology 
Grandparent Node:
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Phenotypic abnormality (HP:0000118)help
Parent Node:
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Constitutional symptom (HP:0025142)help
..Starting node
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Shivering (HP:0025144)help
Term ID: 25144
Name: Shivering
Synonym: Shivering; Shuddering
Definition: Involuntary contraction or twitching of the muscles.
Comments:
Reference: HP:0025144
Genes and Diseases:
 
       Child Nodes:
........expandRigors (HP:0025145) help

 Sister Nodes: 
..expandAsthenia (HP:0025406) help
..expandBody odor (HP:0500001) help
..expandChest tightness (HP:0031352) help
..expandChills (HP:0025143) help
..expandFatigue (HP:0012378) help
..expandHot flashes (HP:0031217) help
..expandImpairment of activities of daily living (HP:0031058) help
..expandNight sweats (HP:0030166) help
..expandPain (HP:0012531) 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:0025144HP:0025144Shivering0CHRNA2 CL E G H11351956OMIM:610353Epilepsy, nocturnal frontal lobe, 4.188
HP:0025144HP:0025144Shivering0HADHA CL E G H30304801ORPHA:746Mitochondrial trifunctional protein deficiency99
HP:0025144HP:0025144Shivering0HADHB CL E G H30324803ORPHA:746Mitochondrial trifunctional protein deficiency60
HP:0025144HP:0025145Rigors1HADHA CL E G H30304801ORPHA:746Mitochondrial trifunctional protein deficiencyHP:0040284 - Very rare99
HP:0025144HP:0025145Rigors1HADHB CL E G H30324803ORPHA:746Mitochondrial trifunctional protein deficiencyHP:0040284 - Very rare60


Genes (3) :CHRNA2 HADHA HADHB

Diseases (2) :OMIM:610353 ORPHA:746
 

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