Human Phenotype Ontology 
Grandparent Node:
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Abnormality of 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 entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012513HP:0012513Upper limb pain0FLI1 CL E G H2313370348ORPHA01743749193067
HP:0012513HP:0012513Upper limb pain0FLI1 CL E G H2313370348ORPHA01723749193067
HP:0012513HP:0012513Upper limb pain0MFN2 CL E G H992799947ORPHA082416877608507
HP:0012513HP:0012513Upper limb pain0MFN2 CL E G H992799947ORPHA094416877608507
HP:0012513HP:0046505Hand pain1FLI1 CL E G H2313370348ORPHA01723749193067
HP:0012513HP:0030836Wrist pain1FLI1 CL E G H2313370348ORPHA01723749193067
HP:0012513HP:0030835Elbow pain1FLI1 CL E G H2313370348ORPHA01743749193067
HP:0012513HP:0030835Elbow pain1FLI1 CL E G H2313370348ORPHA01723749193067
HP:0012513HP:0046505Hand pain1FLI1 CL E G H2313370348ORPHA01743749193067
HP:0012513HP:0030836Wrist pain1FLI1 CL E G H2313370348ORPHA01743749193067
HP:0012513HP:0030835Elbow pain1MFN2 CL E G H992799947ORPHA082416877608507
HP:0012513HP:0046505Hand pain1MFN2 CL E G H992799947ORPHA094416877608507
HP:0012513HP:0030836Wrist pain1MFN2 CL E G H992799947ORPHA094416877608507
HP:0012513HP:0030836Wrist pain1MFN2 CL E G H992799947ORPHA082416877608507
HP:0012513HP:0046505Hand pain1MFN2 CL E G H992799947ORPHA082416877608507
HP:0012513HP:0030835Elbow pain1MFN2 CL E G H992799947ORPHA094416877608507
HP:0012513HP:0030837Finger pain2FLI1 CL E G H2313370348ORPHA01743749193067
HP:0012513HP:0030837Finger pain2FLI1 CL E G H2313370348ORPHA01723749193067
HP:0012513HP:0030837Finger pain2MFN2 CL E G H992799947ORPHA082416877608507
HP:0012513HP:0030837Finger pain2MFN2 CL E G H992799947ORPHA094416877608507


Genes (2) :FLI1 MFN2

Diseases (2) :370348 99947
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.