Myalgia

Symptom Information:

Symptom ID: HPO:0003326
Synonyms:
Muscle pain [HPO:0003326]
MYALGIAS [HPO:0003326]
Muscle pain (finding) [Orphanet:44350]
Myalgia [Orphanet:44350]
Muscle pain [OMIM:Muscle pain]
Myalgia [OMIM:Myalgia]
Myalgias [OMIM:Myalgias]
Myalgia/muscular pain [Orphanet:44350]
Myalgia [MedDRA:10028411]
Generalised muscle aches [MedDRA:10028411]
Muscle ache [MedDRA:10028411]
Muscle pain [MedDRA:10028411]
Muscle soreness [MedDRA:10028411]
Muscle tenderness any site [MedDRA:10028411]
Muscular pain [MedDRA:10028411]
Muscular pains [MedDRA:10028411]
Pain muscle [MedDRA:10028411]
Polymyalgia [MedDRA:10028411]
Polymyalgia aggravated [MedDRA:10028411]
Polymyalgia worsened [MedDRA:10028411]
Tenderness muscle [MedDRA:10028411]
Myalgia aggravated [MedDRA:10028411]
Myalgia of lower extremities [MedDRA:10028411]
Generalized muscle aches [MedDRA:10028411]
Localised muscle pain [MedDRA:10028411]
Localized muscle pain [MedDRA:10028411]
Muscle pain (less common) [OMIM:Muscle pain (less common)]
Myalgia (in some patients) [OMIM:Myalgia (in some patients)]
Muscle pains [MedDRA:10028323]
Quality:
Cross references:
Orphanet:44350 "Myalgia/muscular pain" [Orphanet:44350]
OMIM: "Muscle pain" [OMIM:Muscle pain]
OMIM: "Myalgia" [OMIM:Myalgia]
OMIM: "Myalgias" [OMIM:Myalgias]
OMIM: "Muscle pain (less common)" [OMIM:Muscle pain (less common)]
OMIM: "Myalgia (in some patients)" [OMIM:Myalgia (in some patients)]
UMLS:C0231528 "Myalgia" [Orphanet:44350]
Is a (Direct Parents):
HPO         Abnormality of muscle physiology
MedDRA Muscle disorders
Orphanet Muscle anomalies
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Myalgia(HPO:0003326)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Muscle disorders(MedDRA:10028302)
       Myalgia(HPO:0003326)
Database Frequency: 143 / 7739
Resource:

All diseases associated with this symptom:

AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS (OMIM:616050)
Acetazolamide-responsive myotonia (Orphanet:99736)
Acute intermittent porphyria (Orphanet:79276)
Adult Still's disease (Orphanet:829)
Alström syndrome (Orphanet:64)
Anti-glomerular basement membrane disease (Orphanet:375)
Antisynthetase syndrome (Orphanet:81)
Autosomal dominant limb-girdle muscular dystrophy type 1C (Orphanet:265)
Autosomal dominant myoglobinuria (Orphanet:99846)
Autosomal recessive limb-girdle muscular dystrophy type 2E (Orphanet:119)
Autosomal recessive limb-girdle muscular dystrophy type 2F (Orphanet:219)
Autosomal recessive limb-girdle muscular dystrophy type 2I (Orphanet:34515)
Autosomal recessive limb-girdle muscular dystrophy type 2L (Orphanet:206549)
Autosomal recessive limb-girdle muscular dystrophy type 2S (Orphanet:369840)
BRITTLE CORNEA SYNDROME 2 (OMIM:614170)
Babesiosis (Orphanet:108)
Behçet disease (Orphanet:117)
Brittle cornea syndrome (Orphanet:90354)
Bronchiolitis obliterans with obstructive pulmonary disease (Orphanet:1303)
Buschke-Ollendorff syndrome (Orphanet:1306)
CINCA syndrome (Orphanet:1451)
Carbamoylphosphate synthetase deficiency (Orphanet:147)
Carnitine palmitoyl transferase II deficiency (Orphanet:157)
Carnitine palmitoyl transferase II deficiency, myopathic form (Orphanet:228302)
Childhood-onset hypophosphatasia (Orphanet:247667)
Cogan syndrome (Orphanet:1467)
Congenital muscular dystrophy with cerebellar involvement (Orphanet:370959)
Congenital myopathy with internal nuclei and atypical cores (Orphanet:319160)
Crimean-Congo hemorrhagic fever (Orphanet:99827)
Cryoglobulinemic vasculitis (Orphanet:91138)
Cutaneous leukocytoclastic angiitis (Orphanet:889)
DK1-CDG (Orphanet:91131)
Dermatomyositis (Orphanet:221)
Desmoid tumor (Orphanet:873)
Ebola hemorrhagic fever (Orphanet:319218)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Eosinophilic fasciitis (Orphanet:3165)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Erythema elevatum diutinum (Orphanet:90000)
Fabry disease (Orphanet:324)
Familial Mediterranean fever (Orphanet:342)
Familial cold urticaria (Orphanet:47045)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Febrile infection-related epilepsy syndrome (Orphanet:163703)
Focal myositis (Orphanet:48918)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Genetic recurrent myoglobinuria (Orphanet:99845)
Giant cell arteritis (Orphanet:397)
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency (Orphanet:284426)
Glycogen storage disease due to lactate dehydrogenase deficiency (Orphanet:2364)
Glycogen storage disease due to muscle and heart glycogen synthase deficiency (Orphanet:137625)
Glycogen storage disease due to muscle beta-enolase deficiency (Orphanet:99849)
Glycogen storage disease due to phosphoglycerate mutase deficiency (Orphanet:97234)
Granulomatosis with polyangiitis (Orphanet:900)
Hemorrhagic fever - renal syndrome (Orphanet:340)
Hereditary coproporphyria (Orphanet:79273)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Hyperkalemic periodic paralysis (Orphanet:682)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
Idiopathic acute eosinophilic pneumonia (Orphanet:724)
Idiopathic hypereosinophilic syndrome (Orphanet:3260)
Immunoglobulin A vasculitis (Orphanet:761)
Inclusion body myositis (Orphanet:611)
Juvenile dermatomyositis (Orphanet:93672)
Kerion celsi (Orphanet:499)
Laing distal myopathy (Orphanet:59135)
Lassa fever (Orphanet:99824)
Legionellosis (Orphanet:549)
Lujo hemorrhagic fever (Orphanet:319213)
Lyme disease (Orphanet:91546)
MELAS (Orphanet:550)
MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE) (OMIM:615418)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 (OMIM:606612)
MYOGLOBINURIA, ACUTE RECURRENT, AUTOSOMAL RECESSIVE (OMIM:268200)
MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES (OMIM:616231)
MYOTONIA CONGENITA, AUTOSOMAL DOMINANT (OMIM:160800)
MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE (OMIM:255700)
Macrophagic myofasciitis (Orphanet:592)
Majeed syndrome (Orphanet:77297)
Marburg hemorrhagic fever (Orphanet:99826)
Marfan syndrome (Orphanet:558)
Maternally-inherited cardiomyopathy and hearing loss (Orphanet:1349)
Maternally-inherited diabetes and deafness (Orphanet:225)
Microscopic polyangiitis (Orphanet:727)
Mitochondrial DNA deletion syndrome with progressive myopathy (Orphanet:352470)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Mitochondrial trifunctional protein deficiency (Orphanet:746)
Mixed connective tissue disease (Orphanet:809)
Muckle-Wells syndrome (Orphanet:575)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Muscular pseudohypertrophy - hypothyroidism (Orphanet:2349)
Myopathy due to myoadenylate deaminase deficiency (OMIM:615511)
Myotilin-related myofibrillar myopathy without spheroid body (Orphanet:98911)
Myotonia fluctuans (Orphanet:99734)
Myotonia permanens (Orphanet:99735)
NLRP12-associated hereditary periodic fever syndrome (Orphanet:247868)
Neurogenic thoracic outlet syndrome (Orphanet:100073)
Neutral lipid storage myopathy (Orphanet:98908)
Nipah virus disease (Orphanet:99825)
Nodular non-suppurative panniculitis (Orphanet:33577)
POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY (OMIM:615895)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 (OMIM:609286)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 4 (OMIM:610131)
Paramyotonia congenita of Von Eulenburg (Orphanet:684)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Polyglucosan body myopathy type 1 (ORPHA:397937)
Polymyositis (Orphanet:732)
Pontiac fever (Orphanet:99748)
Potassium-aggravated myotonia (Orphanet:612)
Primary erythermalgia (Orphanet:90026)
Primary hyperoxaluria type 1 (Orphanet:93598)
Primary lipodystrophy (Orphanet:90970)
Primary orthostatic tremor (Orphanet:238606)
Proximal myotonic myopathy (Orphanet:606)
Pyomyositis (Orphanet:764)
Reynolds syndrome (Orphanet:779)
Rift valley fever (Orphanet:319251)
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET (OMIM:615934)
Schnitzler syndrome (Orphanet:37748)
Schwartz-Jampel syndrome (Orphanet:800)
Scleroderma (Orphanet:801)
Scrub typhus (Orphanet:83317)
Sodium channelopathy-related small fiber neuropathy (Orphanet:306577)
Stormorken-Sjaastad-Langslet syndrome (Orphanet:3204)
Sweet syndrome (Orphanet:3243)
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers (Orphanet:206546)
Systemic capillary leak syndrome (Orphanet:188)
Systemic mastocytosis (Orphanet:2467)
TRAPS syndrome (Orphanet:32960)
Takayasu arteritis (Orphanet:3287)
Thomsen and Becker disease (Orphanet:614)
Thoracic outlet syndrome (Orphanet:97330)
Typhoid (Orphanet:99745)
Very long chain acyl-CoA dehydrogenase deficiency (Orphanet:26793)
Viral hemorrhagic fever (Orphanet:341)
Whipple disease (Orphanet:3452)
Yellow fever (Orphanet:99829)
[DEL] MUSCULAR DYSTROPHY, BECKER TYPE (OMIM:300376)