Human Phenotype Ontology 
Grandparent Node:
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Constitutional symptom (HP:0025142)help
Parent Node:
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Abnormal eye physiology (HP:0012373)help
Parent Node:
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Pain (HP:0012531)help
..Starting node
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Ocular pain (HP:0200026)help
Term ID: 200026
Name: Ocular pain
Synonym: Eye pain
Definition: An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the eye.
Comments:
Reference: HP:0200026
Genes and Diseases:
 
       Child Nodes:
........expandEye movement-induced pain (HP:0030857) help

 Sister Nodes: 
..expandAbdominal pain (HP:0002027) help
..expandAllodynia (HP:0012533) help
..expandAnal pain (HP:0500005) help
..expandAnkle pain (HP:0030840) help
..expandArthralgia (HP:0002829) help
..expandBack pain (HP:0003418) help
..expandBone pain (HP:0002653) help
..expandChest pain (HP:0100749) help
..expandChronic pain (HP:0012532) help
..expandCostochondral pain (HP:0006649) help
..expandEar pain (HP:0030766) help
..expandElbow pain (HP:0030835) help
..expandEpigastric pain (HP:0410019) help
..expandFinger pain (HP:0030837) help
..expandFlank pain (HP:0030157) help
..expandFoot pain (HP:0025238) help
..expandGroin pain (HP:0031520) help
..expandHip pain (HP:0030838) help
..expandJaw pain (HP:0040264) help
..expandKnee pain (HP:0030839) help
..expandLimb pain (HP:0009763) help
..expandMandibular pain (HP:0200025) help
..expandMyalgia (HP:0003326) help
..expandNeck pain (HP:0030833) help
..expandScrotal pain (HP:0030155) help
..expandShoulder pain (HP:0030834) help
..expandToe pain (HP:0030841) help
..expandVulvodynia (HP:0030943) help
..expandWrist pain (HP:0030836) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0200026HP:0200026Ocular pain0SCN9A CL E G H6335167400Paroxysmal extreme pain disorder167400C1833661OMIM1129142710597603415
HP:0200026HP:0200026Ocular pain1SCN9A CL E G H6335167400Paroxysmal extreme pain disorder167400C1833661OMIM1129142710597603415
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0200026HP:0200026Ocular pain0BAP1 CL E G H831439044ORPHA01191483950603089
HP:0200026HP:0200026Ocular pain0CYSLTR2 CL E G H5710539044ORPHA026318274605666
HP:0200026HP:0200026Ocular pain0GNA11 CL E G H276739044ORPHA0111284379139313
HP:0200026HP:0200026Ocular pain0GNAQ CL E G H277639044ORPHA06724390600998
HP:0200026HP:0200026Ocular pain0SF3B1 CL E G H2345139044ORPHA046710768605590
HP:0200026HP:0200026Ocular pain0SLC39A14 CL E G H23516144755Hyperostosis cranialis interna144755C1840404OMIM0913620858608736
HP:0200026HP:0200026Ocular pain1BAP1 CL E G H831439044ORPHA01191483950603089
HP:0200026HP:0200026Ocular pain1CYSLTR2 CL E G H5710539044ORPHA026318274605666
HP:0200026HP:0200026Ocular pain1GNA11 CL E G H276739044ORPHA0111284379139313
HP:0200026HP:0200026Ocular pain1GNAQ CL E G H277639044ORPHA06724390600998
HP:0200026HP:0200026Ocular pain1SF3B1 CL E G H2345139044ORPHA046710768605590
HP:0200026HP:0200026Ocular pain1SLC39A14 CL E G H23516144755Hyperostosis cranialis interna144755C1840404OMIM0913620858608736


Genes (7) :BAP1 CYSLTR2 GNA11 GNAQ SCN9A SF3B1 SLC39A14

Diseases (3) :39044 167400 144755
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.