Human Phenotype Ontology 
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Ocular flutter (HP:0031931)help
Term ID: 31931
Name: Ocular flutter
Synonym:
Definition: Ocular flutter is an abnormal eye movement consisting of repetitive, irregular, involuntary bursts of horizontal saccades without an intersaccadic interval. It is generally superimposed on normal oculomotor behaviour and its occurrence may be favoured by various events, such as blinks, the triggering of normal saccades or optokinetic stimulation.
Comments:
Reference: HP:0031931
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:0031931HP:0031931Ocular flutter0ATP1A2 CL E G H477800ORPHA:2131Alternating hemiplegia of childhoodHP:0040283 - Occasional239
HP:0031931HP:0031931Ocular flutter0ATP1A3 CL E G H478801ORPHA:2131Alternating hemiplegia of childhoodHP:0040283 - Occasional150
HP:0031931HP:0031931Ocular flutter0CACNA1A CL E G H7731388ORPHA:2131Alternating hemiplegia of childhoodHP:0040283 - Occasional449
HP:0031931HP:0031931Ocular flutter0SLC1A3 CL E G H650710941ORPHA:2131Alternating hemiplegia of childhoodHP:0040283 - Occasional63
HP:0031931HP:0031931Ocular flutter0SLC35A2 CL E G H735511022OMIM:300896Congenital disorder of glycosylation, type IIm.27
HP:0031931HP:0031931Ocular flutter0SLC6A3 CL E G H653111049OMIM:613135Parkinsonism-Dystonia, infantile, 1.13


Genes (6) :ATP1A2 ATP1A3 CACNA1A SLC1A3 SLC35A2 SLC6A3

Diseases (3) :ORPHA:2131 OMIM:300896 OMIM:613135
 

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