Arthralgia

Symptom Information:

Symptom ID: HPO:0002829
Synonyms:
Arthralgias [HPO:0002829]
Joint pain [HPO:0002829]
JOINT PAINS [HPO:0002829]
Joint pain (finding) [Orphanet:46040]
Arthralgia [Orphanet:46040]
Arthralgia [OMIM:Arthralgia]
Arthralgias [OMIM:Arthralgias]
Joint pain [OMIM:Joint pain]
Articular/joint pain/arthralgia [Orphanet:46040]
Arthralgia [MedDRA:10003239]
Ache wrists [MedDRA:10003239]
Aching (l) knee [MedDRA:10003239]
Aching (r) knee [MedDRA:10003239]
Aching in knees [MedDRA:10003239]
Aching joints [MedDRA:10003239]
Arthralgia aggravated [MedDRA:10003239]
Arthralgia lumbar [MedDRA:10003239]
Arthralgia multiple [MedDRA:10003239]
Arthritic pains [MedDRA:10003239]
Arthritic-like pain [MedDRA:10003239]
Burning sensation in joints [MedDRA:10003239]
Coxalgia [MedDRA:10003239]
Generalised joint pains [MedDRA:10003239]
Joint ache [MedDRA:10003239]
Joint pain [MedDRA:10003239]
Knee pain [MedDRA:10003239]
Pain ankle [MedDRA:10003239]
Pain in (l) elbow [MedDRA:10003239]
Pain in (l) hip [MedDRA:10003239]
Pain in (l) knee [MedDRA:10003239]
Pain in (r) elbow [MedDRA:10003239]
Pain in (r) hip [MedDRA:10003239]
Pain in (r) knee [MedDRA:10003239]
Pain in ankle [MedDRA:10003239]
Pain in elbow [MedDRA:10003239]
Pain in hip [MedDRA:10003239]
Pain in joint [MedDRA:10003239]
Pain in joint involving ankle and foot [MedDRA:10003239]
Pain in joint involving forearm [MedDRA:10003239]
Pain in joint involving hand [MedDRA:10003239]
Pain in joint involving lower leg [MedDRA:10003239]
Pain in joint involving multiple sites [MedDRA:10003239]
Pain in joint involving other specified sites [MedDRA:10003239]
Pain in joint involving pelvic region and thigh [MedDRA:10003239]
Pain in joint involving shoulder region [MedDRA:10003239]
Pain in joint involving upper arm [MedDRA:10003239]
Pain in joint, site unspecified [MedDRA:10003239]
Pain in knee [MedDRA:10003239]
Pain joint [MedDRA:10003239]
Pain knee [MedDRA:10003239]
Pain sacroiliac [MedDRA:10003239]
Painful ankle [MedDRA:10003239]
Painful hips [MedDRA:10003239]
Painful joints [MedDRA:10003239]
Painful knee [MedDRA:10003239]
Polyarthralgia [MedDRA:10003239]
Rheumatism (joints only) [MedDRA:10003239]
Sacro-iliac pain [MedDRA:10003239]
Shoulder joint pain associated with [MedDRA:10003239]
Shoulder pain (due joint disorder) [MedDRA:10003239]
Wrist pain [MedDRA:10003239]
Joint tenderness [MedDRA:10003239]
Generalized joint pain [MedDRA:10003239]
Gonalgia [MedDRA:10003239]
Burning sensation in joints worsened [MedDRA:10003239]
Coxodynia [MedDRA:10003239]
Generalised joint pain [MedDRA:10003239]
Arthralgia (hands, feet, ankles, and knees) [OMIM:Arthralgia (hands, feet, ankles, and knees)]
Arthralgia (in some patients) [OMIM:Arthralgia (in some patients)]
Arthralgia (knee) [OMIM:Arthralgia (knee)]
Arthralgias (hips, knees) [OMIM:Arthralgias (hips, knees)]
Arthralgias (knees and shoulders) [OMIM:Arthralgias (knees and shoulders)]
Arthralgias (knees) [OMIM:Arthralgias (knees)]
Arthralgias (onset early school age) [OMIM:Arthralgias (onset early school age)]
Joint pain (late-onset) [OMIM:Joint pain (late-onset)]
Joint pains [OMIM:Joint pains]
Knee pain [OMIM:Knee pain]
Painful joints [OMIM:Painful joints]
Wrist pain [OMIM:Wrist pain]
Quality:
Cross references:
HPO:0005059 "arthralgia/arthritis" [Orphanet:46040]
Orphanet:46040 "Articular/joint pain/arthralgia" [Orphanet:46040]
OMIM: "Arthralgia" [OMIM:Arthralgia]
OMIM: "Arthralgias" [OMIM:Arthralgias]
OMIM: "Joint pain" [OMIM:Joint pain]
OMIM: "Arthralgia (hands, feet, ankles, and knees)" [OMIM:Arthralgia (hands, feet, ankles, and knees)]
OMIM: "Arthralgia (in some patients)" [OMIM:Arthralgia (in some patients)]
OMIM: "Arthralgia (knee)" [OMIM:Arthralgia (knee)]
OMIM: "Arthralgias (hips, knees)" [OMIM:Arthralgias (hips, knees)]
OMIM: "Arthralgias (knees and shoulders)" [OMIM:Arthralgias (knees and shoulders)]
OMIM: "Arthralgias (knees)" [OMIM:Arthralgias (knees)]
OMIM: "Arthralgias (onset early school age)" [OMIM:Arthralgias (onset early school age)]
OMIM: "Joint pain (late-onset)" [OMIM:Joint pain (late-onset)]
OMIM: "Joint pains" [OMIM:Joint pains]
OMIM: "Knee pain" [OMIM:Knee pain]
OMIM: "Painful joints" [OMIM:Painful joints]
OMIM: "Wrist pain" [OMIM:Wrist pain]
UMLS:C0003862 "Arthralgia" [HPO:0002829]
UMLS:C0003862 "Arthralgia" [Orphanet:46040]
Is a (Direct Parents):
HPO         Abnormal joint morphology
Orphanet Abnormal cartilage morphology
MedDRA Joint related signs and symptoms
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal joint morphology(HPO:0001367)
                Arthralgia(HPO:0002829)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Joint disorders(MedDRA:10023213)
       Joint related signs and symptoms(MedDRA:10023226)
          Arthralgia(HPO:0002829)
Database Frequency: 79 / 7739
Resource:

All diseases associated with this symptom:

AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III (OMIM:615559)
AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS (OMIM:616050)
Adiposis dolorosa (Orphanet:36397)
Alkaptonuria (Orphanet:56)
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation (Orphanet:324530)
Autosomal dominant spastic paraplegia type 8 (Orphanet:100989)
Buschke-Ollendorff syndrome (Orphanet:1306)
CANDLE syndrome (Orphanet:325004)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
CHILBLAIN LUPUS 1 (OMIM:610448)
CHST3-related skeletal dysplasia (Orphanet:263463)
COMPLEMENT COMPONENT C1r/C1s DEFICIENCY (OMIM:216950)
CREST syndrome (Orphanet:90290)
Carney complex (Orphanet:1359)
Chilblain lupus (Orphanet:90280)
Cranio-osteoarthropathy (Orphanet:1525)
Czech dysplasia, metatarsal type (Orphanet:137678)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Diffuse cutaneous systemic sclerosis (Orphanet:220393)
EPIPHYSEAL DYSPLASIA, MULTIPLE, 6 (OMIM:614135)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4 (OMIM:616115)
FAMILIAL MEDITERRANEAN FEVER (OMIM:249100)
FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT (OMIM:134610)
Fabry disease (Orphanet:324)
Familial Mediterranean fever (Orphanet:342)
Familial cold urticaria (Orphanet:47045)
HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2 (OMIM:614441)
Hemochromatosis type 2 (Orphanet:79230)
Hemochromatosis type 3 (Orphanet:225123)
Hemochromatosis type 4 (Orphanet:139491)
Hemochromatosis, type 2A (OMIM:602390)
Hemochromatosis, type 2B (OMIM:613313)
Hereditary arterial and articular multiple calcification syndrome (Orphanet:289601)
Hurler-Scheie syndrome (Orphanet:93476)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1 (OMIM:161950)
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2 (OMIM:613944)
JMP syndrome (Orphanet:324999)
Kniest dysplasia (Orphanet:485)
Limited cutaneous systemic sclerosis (Orphanet:220402)
MUCOLIPIDOSIS III GAMMA (OMIM:252605)
Mediterranean macrothrombocytopenia (Orphanet:101022)
Mevalonic aciduria (Orphanet:29)
Muckle-Wells syndrome (Orphanet:575)
Multicentric carpo-tarsal osteolysis with or without nephropathy (Orphanet:2774)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Multiple epiphyseal dysplasia type 4 (Orphanet:93307)
Multiple epiphyseal dysplasia type 5 (Orphanet:93311)
Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia (Orphanet:166029)
NLRP12-associated hereditary periodic fever syndrome (Orphanet:247868)
Nakajo-Nishimura syndrome (Orphanet:2615)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)
Non-specific interstitial pneumonia (Orphanet:91364)
OSTEOARTHRITIS SUSCEPTIBILITY 3 (OMIM:607850)
Otospondylomegaepiphyseal dysplasia (Orphanet:1427)
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2 (OMIM:615399)
Partial acquired lipodystrophy (Orphanet:79087)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Pediatric systemic sclerosis (Orphanet:93567)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Primary hyperoxaluria type 1 (Orphanet:93598)
Proteasome disability syndrome (Orphanet:324977)
Pseudoachondroplasia (Orphanet:750)
Pyle disease (Orphanet:3005)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED (OMIM:313400)
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET (OMIM:615934)
SYNOVIAL CHONDROMATOSIS, FAMILIAL, WITH DWARFISM (OMIM:186575)
Spondyloepimetaphyseal dysplasia, Irapa type (Orphanet:93351)
Sterile multifocal osteomyelitis with periostitis and pustulosis (Orphanet:210115)
Stickler syndrome type 3 (Orphanet:166100)
TRAPS syndrome (Orphanet:32960)
TRICHORHINOPHALANGEAL SYNDROME, TYPE I (OMIM:190350)
Torg-Winchester syndrome (Orphanet:3460)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Ulna metaphyseal dysplasia syndrome (Orphanet:1837)
Upington disease (Orphanet:3408)
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR (OMIM:600785)
X-linked hypophosphatemia (Orphanet:89936)