Human Phenotype Ontology 
Grandparent Node:
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Constitutional symptom (HP:0025142)help
Parent Node:
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Abnormal ear physiology (HP:0031704)help
Parent Node:
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Pain (HP:0012531)help
..Starting node
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Ear pain (HP:0030766)help
Term ID: 30766
Name: Ear pain
Synonym: Ear pain; Otalgia; Pain in the ear
Definition: Pain in the ear can be a consequence of otologic disease (primary or otogenic otalgia), or can arise from pathologic processes and structures other than the ear (secondary or referred otalgia).
Comments:
Reference: HP:0030766
Genes and Diseases:
 
       Child Nodes:

 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
..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
..expandOcular pain (HP:0200026) 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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030766HP:0030766Ear pain0AKT1 CL E G H207391ORPHA:2495MeningiomaHP:0040284 - Very rare54
HP:0030766HP:0030766Ear pain0BAP1 CL E G H8314950ORPHA:2495MeningiomaHP:0040284 - Very rare184
HP:0030766HP:0030766Ear pain0KRT16 CL E G H38686423ORPHA:2309Pachyonychia congenitaHP:0040283 - Occasional27
HP:0030766HP:0030766Ear pain0KRT17 CL E G H38726427ORPHA:2309Pachyonychia congenitaHP:0040283 - Occasional23
HP:0030766HP:0030766Ear pain0KRT6A CL E G H38536443ORPHA:2309Pachyonychia congenitaHP:0040283 - Occasional41
HP:0030766HP:0030766Ear pain0KRT6B CL E G H38546444ORPHA:2309Pachyonychia congenitaHP:0040283 - Occasional4
HP:0030766HP:0030766Ear pain0NF2 CL E G H47717773ORPHA:2495MeningiomaHP:0040284 - Very rare220
HP:0030766HP:0030766Ear pain0PDGFB CL E G H51558800ORPHA:2495MeningiomaHP:0040284 - Very rare9
HP:0030766HP:0030766Ear pain0PIK3CA CL E G H52908975ORPHA:2495MeningiomaHP:0040284 - Very rare162
HP:0030766HP:0030766Ear pain0SMARCB1 CL E G H659811103ORPHA:2495MeningiomaHP:0040284 - Very rare87
HP:0030766HP:0030766Ear pain0SMARCE1 CL E G H660511109ORPHA:2495MeningiomaHP:0040284 - Very rare47
HP:0030766HP:0030766Ear pain0SMO CL E G H660811119ORPHA:2495MeningiomaHP:0040284 - Very rare22
HP:0030766HP:0030766Ear pain0SUFU CL E G H5168416466ORPHA:2495MeningiomaHP:0040284 - Very rare124
HP:0030766HP:0030766Ear pain0TERT CL E G H701511730ORPHA:2495MeningiomaHP:0040284 - Very rare238
HP:0030766HP:0030766Ear pain0TRAF7 CL E G H8423120456ORPHA:2495MeningiomaHP:0040284 - Very rare


Genes (15) :AKT1 BAP1 KRT16 KRT17 KRT6A KRT6B NF2 PDGFB PIK3CA SMARCB1 SMARCE1 SMO SUFU TERT TRAF7

Diseases (2) :ORPHA:2495 ORPHA:2309
 

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