Human Phenotype Ontology 
Grandparent Node:
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Abnormal eye physiology (HP:0012373)help
Grandparent Node:
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Pain (HP:0012531)help
Parent Node:
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Ocular pain (HP:0200026)help
..Starting node
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Eye movement-induced pain (HP:0030857)help
Term ID: 30857
Name: Eye movement-induced pain
Synonym:
Definition: An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the eye that is worse in certain directions of gaze and during prolonged gaze holding.
Comments:
Reference: HP:0030857
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:0030857HP:0030857Eye movement-induced pain0AGBL1 CL E G H12362426504ORPHA:98974Fuchs endothelial corneal dystrophy3
HP:0030857HP:0030857Eye movement-induced pain0COL8A2 CL E G H12962216ORPHA:98974Fuchs endothelial corneal dystrophy3
HP:0030857HP:0030857Eye movement-induced pain0SLC4A11 CL E G H8395916438ORPHA:98974Fuchs endothelial corneal dystrophy66
HP:0030857HP:0030857Eye movement-induced pain0TCF4 CL E G H692511634ORPHA:98974Fuchs endothelial corneal dystrophy241
HP:0030857HP:0030857Eye movement-induced pain0ZEB1 CL E G H693511642ORPHA:98974Fuchs endothelial corneal dystrophy8


Genes (5) :AGBL1 COL8A2 SLC4A11 TCF4 ZEB1

Diseases (1) :ORPHA:98974
 

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