Human Phenotype Ontology 
Grandparent Node:
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Abnormal musculoskeletal physiology (HP:0011843)help
Grandparent Node:
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Pain (HP:0012531)help
Parent Node:
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Limb pain (HP:0009763)help
..Starting node
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Upper limb pain (HP:0012513)help
Term ID: 12513
Name: Upper limb pain
Synonym: Upper limb pain
Definition: An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the arm.
Comments:
Reference: HP:0012513
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandLower limb pain (HP:0012514) 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:0012513HP:0012513Upper limb pain0B2M CL E G H567914ORPHA:314652Variant ABeta2M amyloidosis8
HP:0012513HP:0012513Upper limb pain0COMP CL E G H13112227OMIM:619161CARPAL TUNNEL SYNDROME 2; CTS289
HP:0012513HP:0012513Upper limb pain0FLI1 CL E G H23133749ORPHA:370348Peripheral primitive neuroectodermal tumorHP:0040283 - Occasional8
HP:0012513HP:0012513Upper limb pain0IDUA CL E G H34255391OMIM:607015Hurler-Scheie syndrome115
HP:0012513HP:0012513Upper limb pain0KRT14 CL E G H38616416ORPHA:79400Localized epidermolysis bullosa simplexHP:0040282 - Frequent110
HP:0012513HP:0012513Upper limb pain0KRT5 CL E G H38526442ORPHA:79400Localized epidermolysis bullosa simplexHP:0040282 - Frequent173
HP:0012513HP:0012513Upper limb pain0MAFB CL E G H99356408OMIM:166300Multicentric carpotarsal osteolysis syndrome63
HP:0012513HP:0012513Upper limb pain0MFN2 CL E G H992716877ORPHA:99947Autosomal dominant Charcot-Marie-Tooth disease type 2A2HP:0040283 - Occasional203
HP:0012513HP:0030835Elbow pain1 CL E G H
HP:0012513HP:0030836Wrist pain1B2M CL E G H567914ORPHA:314652Variant ABeta2M amyloidosisHP:0040283 - Occasional8
HP:0012513HP:0046505Hand pain1COMP CL E G H13112227OMIM:619161CARPAL TUNNEL SYNDROME 2; CTS289
HP:0012513HP:0046505Hand pain1IDUA CL E G H34255391OMIM:607015Hurler-Scheie syndrome115
HP:0012513HP:0030836Wrist pain1MAFB CL E G H99356408OMIM:166300Multicentric carpotarsal osteolysis syndrome63
HP:0012513HP:0030837Finger pain2 CL E G H


Genes (8) :B2M COMP FLI1 IDUA KRT14 KRT5 MAFB MFN2

Diseases (7) :ORPHA:314652 OMIM:619161 ORPHA:370348 OMIM:607015 ORPHA:79400 OMIM:166300 ORPHA:99947
 

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