Human Phenotype Ontology 
Grandparent Node:
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Abnormal muscle physiology (HP:0011804)help
Parent Node:
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EMG abnormality (HP:0003457)help
..Starting node
..expand
EMG: continuous motor unit activity at rest (HP:0100283)help
Term ID: 100283
Name: EMG: continuous motor unit activity at rest
Synonym:
Definition: Continuous electromyographic activity of motor units at rest, i.e., without voluntary movement of the muscles.
Comments:
Reference: HP:0100283
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEMG: axonal abnormality (HP:0003482) help
..expandEMG: impaired neuromuscular transmission (HP:0100285) help
..expandEMG: myokymic discharges (HP:0100288) help
..expandEMG: myopathic abnormalities (HP:0003458) help
..expandEMG: myotonic discharges (HP:0100284) help
..expandEMG: neuropathic changes (HP:0003445) help
..expandEMG: repetitive nerve stimulation abnormality (HP:0030000) help
..expandEMG: slow motor conduction (HP:0100287) help
..expandSingle fiber EMG abnormality (HP:0030006) 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:0100283HP:0100283EMG: continuous motor unit activity at rest0 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.