Human Phenotype Ontology 
Grandparent Node:
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Abnormality of movement (HP:0100022)help
Parent Node:
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Myokymia (HP:0002411)help
..Starting node
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Eyelid myokymia (HP:0031166)help
Term ID: 31166
Name: Eyelid myokymia
Synonym: Myokymia orbicularis; Orbicularis myokymia
Definition: Involuntary, fine, continuous, undulating contractions of the eyelid.
Comments:
Reference: HP:0031166
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEMG: myokymic discharges (HP:0100288) help
..expandFacial myokymia (HP:0000317) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0031166HP:0031166Eyelid myokymia0CACNA1G CL E G H8913458803ORPHA13741394604065
HP:0031166HP:0031166Eyelid myokymia0CACNA1G CL E G H8913458803ORPHA13571394604065
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031166HP:0031166Eyelid myokymia0CACNA1G CL E G H8913616795Spinocerebellar ataxia 42616795C4225205OMIM03741394604065
HP:0031166HP:0031166Eyelid myokymia0CACNA1G CL E G H8913616795Spinocerebellar ataxia 42616795C4225205OMIM03571394604065


Genes (1) :CACNA1G

Diseases (2) :458803 616795
 

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