Human Phenotype Ontology

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Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Constitutional symptom (HP:0025142)

Parent Node:
Pain (HP:0012531)

..Starting node
..Hip pain (HP:0030838)

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:

Abdominal pain (HP:0002027)

Allodynia (HP:0012533)

Anal pain (HP:0500005)

Ankle pain (HP:0030840)

Arthralgia (HP:0002829)

Back pain (HP:0003418)

Bone pain (HP:0002653)

Chest pain (HP:0100749)

Chronic pain (HP:0012532)

Costochondral pain (HP:0006649)

Ear pain (HP:0030766)

Elbow pain (HP:0030835)

Epigastric pain (HP:0410019)

Finger pain (HP:0030837)

Flank pain (HP:0030157)

Foot pain (HP:0025238)

Groin pain (HP:0031520)

Jaw pain (HP:0040264)

Knee pain (HP:0030839)

Limb pain (HP:0009763)

Mandibular pain (HP:0200025)

Myalgia (HP:0003326)

Neck pain (HP:0030833)

Ocular pain (HP:0200026)

Scrotal pain (HP:0030155)

Shoulder pain (HP:0030834)

Toe pain (HP:0030841)

Vulvodynia (HP:0030943)

Wrist pain (HP:0030836)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030838	HP:0030838	Hip pain	0	BSCL2 CL E G H	26580	15832	ORPHA:100998	Autosomal dominant spastic paraplegia type 17	HP:0040283 - Occasional	105
HP:0030838	HP:0030838	Hip pain	0	COL2A1 CL E G H	1280	2200	OMIM:608805	Avascular necrosis of femoral head, primary, 1		284
HP:0030838	HP:0030838	Hip pain	0	COL2A1 CL E G H	1280	2200	ORPHA:86820	Familial avascular necrosis of femoral head	HP:0040282 - Frequent	284
HP:0030838	HP:0030838	Hip pain	0	COL2A1 CL E G H	1280	2200	ORPHA:94068	Spondyloepiphyseal dysplasia congenita	HP:0040282 - Frequent	284
HP:0030838	HP:0030838	Hip pain	0	HNRNPA1 CL E G H	3178	5031	ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia	HP:0040282 - Frequent	31
HP:0030838	HP:0030838	Hip pain	0	HNRNPA2B1 CL E G H	3181	5033	ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia	HP:0040282 - Frequent	5
HP:0030838	HP:0030838	Hip pain	0	HYAL1 CL E G H	3373	5320	OMIM:601492	Mucopolysaccharidosis type IX		28
HP:0030838	HP:0030838	Hip pain	0	LEMD3 CL E G H	23592	28887	ORPHA:166119	Isolated osteopoikilosis		68
HP:0030838	HP:0030838	Hip pain	0	LMNA CL E G H	4000	6636	ORPHA:740	Hutchinson-Gilford progeria syndrome	HP:0040283 - Occasional	645
HP:0030838	HP:0030838	Hip pain	0	MATN3 CL E G H	4148	6909	OMIM:607078	Epiphyseal dysplasia, multiple, 5		32
HP:0030838	HP:0030838	Hip pain	0	TRPV4 CL E G H	59341	18083	ORPHA:86820	Familial avascular necrosis of femoral head	HP:0040282 - Frequent	214
HP:0030838	HP:0030838	Hip pain	0	VCP CL E G H	7415	12666	OMIM:167320	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1	.	63
HP:0030838	HP:0030838	Hip pain	0	VCP CL E G H	7415	12666	ORPHA:52430	Inclusion body myopathy with Paget disease of bone and frontotemporal dementia	HP:0040282 - Frequent	63
HP:0030838	HP:0030838	Hip pain	0	ZMPSTE24 CL E G H	10269	12877	ORPHA:740	Hutchinson-Gilford progeria syndrome	HP:0040283 - Occasional	83

Genes (11) :BSCL2 COL2A1 HNRNPA1 HNRNPA2B1 HYAL1 LEMD3 LMNA MATN3 TRPV4 VCP ZMPSTE24

Diseases (10) :ORPHA:100998 OMIM:608805 ORPHA:86820 ORPHA:94068 ORPHA:52430 OMIM:601492 ORPHA:166119 ORPHA:740 OMIM:607078 OMIM:167320

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

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