Human Phenotype Ontology 
Grandparent Node:
expand
Constitutional symptom (HP:0025142)help
Parent Node:
expand
Pain (HP:0012531)help
..Starting node
..expand
Hip pain (HP:0030838)help
Term ID: 30838
Name: Hip pain
Synonym: Hip pain
Definition: An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the hip.
Comments:
Reference: HP:0030838
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
..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
..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 entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0030838HP:0030838Hip pain0HNRNPA1 CL E G H317852430ORPHA1605031164017
HP:0030838HP:0030838Hip pain0HNRNPA1 CL E G H317852430ORPHA1595031164017
HP:0030838HP:0030838Hip pain0HNRNPA2B1 CL E G H318152430ORPHA11555033600124
HP:0030838HP:0030838Hip pain0HNRNPA2B1 CL E G H318152430ORPHA11265033600124
HP:0030838HP:0030838Hip pain0VCP CL E G H741552430ORPHA139512666601023
HP:0030838HP:0030838Hip pain0VCP CL E G H741552430ORPHA135612666601023
HP:0030838HP:0030838Hip pain0VCP CL E G H7415167320Inclusion body myopathy with early-onset paget disease and frontotemporal dementia167320C1833662OMIM139512666601023
HP:0030838HP:0030838Hip pain0VCP CL E G H7415167320Inclusion body myopathy with early-onset paget disease and frontotemporal dementia167320C1833662OMIM135612666601023
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030838HP:0030838Hip pain0BSCL2 CL E G H26580100998ORPHA037315832606158
HP:0030838HP:0030838Hip pain0BSCL2 CL E G H26580100998ORPHA033015832606158


Genes (4) :BSCL2 HNRNPA1 HNRNPA2B1 VCP

Diseases (3) :100998 52430 167320
 

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