Human Phenotype Ontology 
Grandparent Node:
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Abnormality of movement (HP:0100022)help
Parent Node:
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EMG abnormality (HP:0003457)help
Parent Node:
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Myokymia (HP:0002411)help
..Starting node
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EMG: myokymic discharges (HP:0100288)help
Term ID: 100288
Name: EMG: myokymic discharges
Synonym:
Definition: The presence of spontaneous bursts of rapidly firing potentials that recur at regular intervals of 2-10 per second and are unaffected by voluntary effort. This is an electromyographic (EMG) finding.
Comments:
Reference: HP:0100288
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEyelid myokymia (HP:0031166) help
..expandFacial myokymia (HP:0000317) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0100288HP:0100288EMG: myokymic discharges0HINT1 CL E G H3094324442ORPHA11254912601314
HP:0100288HP:0100288EMG: myokymic discharges0HINT1 CL E G H3094324442ORPHA11144912601314
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :HINT1

Diseases (1) :324442
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.