以 HPO 交叉檢視

HPO → 對應的病歷用詞，並附加具此 HPO 的疾病作為參考。

搜尋 HPO

Arthralgia

HP:0002829

對應病歷用詞(0)

尚無對應用詞。

具此 HPO 的疾病（附加參考）(197)

Generalized pustular psoriasisORPHA:247353 · Obligate (100%)
AcromegalyORPHA:963 · Very frequent (99-80%)
Adiposis dolorosaORPHA:36397 · Very frequent (99-80%)
Adult-onset Still diseaseORPHA:829 · Very frequent (99-80%)
AlkaptonuriaORPHA:56 · Very frequent (99-80%)
ArachnoiditisORPHA:137817 · Very frequent (99-80%)
Autosomal dominant otospondylomegaepiphyseal dysplasiaORPHA:166100 · Very frequent (99-80%)
Blau syndromeORPHA:90340 · Very frequent (99-80%)
Brachydactylous dwarfism, Mseleni typeORPHA:2619 · Very frequent (99-80%)
ChikungunyaORPHA:324625 · Very frequent (99-80%)
CHST3-related skeletal dysplasiaORPHA:263463 · Very frequent (99-80%)
CINCA syndromeORPHA:1451 · Very frequent (99-80%)
Cold agglutinin diseaseORPHA:56425 · Very frequent (99-80%)
Dermatoosteolysis, Kirghizian typeORPHA:1657 · Very frequent (99-80%)
Distal Xq28 microduplication syndromeORPHA:293939 · Very frequent (99-80%)
Drug-induced lupus erythematosusORPHA:231111 · Very frequent (99-80%)
Eiken syndromeORPHA:79106 · Very frequent (99-80%)
Enthesitis-related juvenile idiopathic arthritisORPHA:85438 · Very frequent (99-80%)
Erythema elevatum diutinumORPHA:90000 · Very frequent (99-80%)
Fabry diseaseORPHA:324 · Very frequent (99-80%)
Familial calcium pyrophosphate depositionORPHA:1416 · Very frequent (99-80%)
Familial Mediterranean feverORPHA:342 · Very frequent (99-80%)
Felty syndromeORPHA:47612 · Very frequent (99-80%)
GM1 gangliosidosisORPHA:354 · Very frequent (99-80%)
Granulomatosis with polyangiitisORPHA:900 · Very frequent (99-80%)
Hemophilia AORPHA:98878 · Very frequent (99-80%)
Hyperimmunoglobulinemia D with periodic feverORPHA:343 · Very frequent (99-80%)
Hypermobile Ehlers-Danlos syndromeORPHA:285 · Very frequent (99-80%)
Immunoglobulin A vasculitisORPHA:761 · Very frequent (99-80%)
Kienbock diseaseORPHA:97332 · Very frequent (99-80%)
Ledderhose diseaseORPHA:199251 · Very frequent (99-80%)
Legg-Calvé-Perthes diseaseORPHA:2380 · Very frequent (99-80%)
Macrophagic myofasciitisORPHA:592 · Very frequent (99-80%)
Majeed syndromeORPHA:77297 · Very frequent (99-80%)
Marshall syndromeORPHA:560 · Very frequent (99-80%)
MelorheostosisORPHA:2485 · Very frequent (99-80%)
Muckle-Wells syndromeORPHA:575 · Very frequent (99-80%)
Multiple epiphyseal dysplasia type 4ORPHA:93307 · Very frequent (99-80%)
Multiple symmetric lipomatosisORPHA:2398 · Very frequent (99-80%)
Nasu-Hakola diseaseORPHA:2770 · Very frequent (99-80%)
Neuralgic amyotrophyORPHA:2901 · Very frequent (99-80%)
Neurogenic thoracic outlet syndromeORPHA:100073 · Very frequent (99-80%)
Nodular non-suppurative panniculitisORPHA:33577 · Very frequent (99-80%)
Osteochondritis dissecansORPHA:2764 · Very frequent (99-80%)
Paroxysmal cold hemoglobinuriaORPHA:90035 · Very frequent (99-80%)
PolymyositisORPHA:732 · Very frequent (99-80%)
Pyoderma gangrenosumORPHA:48104 · Very frequent (99-80%)
Reactive arthritisORPHA:29207 · Very frequent (99-80%)
Rheumatoid factor-positive polyarticular juvenile idiopathic arthritisORPHA:85435 · Very frequent (99-80%)
SAPHO syndromeORPHA:793 · Very frequent (99-80%)
Schnitzler syndromeORPHA:37748 · Very frequent (99-80%)
SomatomammotropinomaORPHA:314769 · Very frequent (99-80%)
Spastic paraplegia-Paget disease of bone syndromeORPHA:329475 · Very frequent (99-80%)
Spinal arteriovenous metameric syndromeORPHA:53721 · Very frequent (99-80%)
Spondyloepimetaphyseal dysplasia, Irapa typeORPHA:93351 · Very frequent (99-80%)
Stickler syndromeORPHA:828 · Very frequent (99-80%)
Systemic sclerosisORPHA:90291 · Very frequent (99-80%)
Systemic-onset juvenile idiopathic arthritisORPHA:85414 · Very frequent (99-80%)
Tenosynovial giant cell tumorORPHA:66627 · Very frequent (99-80%)
Whipple diseaseORPHA:3452 · Very frequent (99-80%)
Wilson diseaseORPHA:905 · Very frequent (99-80%)
Xeroderma pigmentosumORPHA:910 · Very frequent (99-80%)
Aggressive systemic mastocytosisORPHA:98850 · Frequent (79-30%)
AngiostrongyliasisORPHA:74 · Frequent (79-30%)
Antisynthetase syndromeORPHA:81 · Frequent (79-30%)
Arthrochalasia Ehlers-Danlos syndromeORPHA:1899 · Frequent (79-30%)
Autoimmune hemolytic anemia, warm typeORPHA:90033 · Frequent (79-30%)
Autoimmune hepatitisORPHA:2137 · Frequent (79-30%)
Autosomal recessive Stickler syndromeORPHA:250984 · Frequent (79-30%)
BabesiosisORPHA:108 · Frequent (79-30%)
Behçet diseaseORPHA:117 · Frequent (79-30%)
Boutonneuse feverORPHA:83313 · Frequent (79-30%)
BrucellosisORPHA:1304 · Frequent (79-30%)
Buerger diseaseORPHA:36258 · Frequent (79-30%)
Catastrophic antiphospholipid syndromeORPHA:464343 · Frequent (79-30%)
Classical-like Ehlers-Danlos syndrome type 1ORPHA:230839 · Frequent (79-30%)
Congenital patella dislocationORPHA:295036 · Frequent (79-30%)
Cranio-osteoarthropathyORPHA:1525 · Frequent (79-30%)
Cryoglobulinemic vasculitisORPHA:91138 · Frequent (79-30%)
Cutaneous small vessel vasculitisORPHA:889 · Frequent (79-30%)
Dengue feverORPHA:99828 · Frequent (79-30%)
DermatomyositisORPHA:221 · Frequent (79-30%)
Diffuse cutaneous systemic sclerosisORPHA:220393 · Frequent (79-30%)
Eosinophilic fasciitisORPHA:3165 · Frequent (79-30%)
Eosinophilic granulomatosis with polyangiitisORPHA:183 · Frequent (79-30%)
Farber diseaseORPHA:333 · Frequent (79-30%)
Gaucher diseaseORPHA:355 · Frequent (79-30%)
Hajdu-Cheney syndromeORPHA:955 · Frequent (79-30%)
Immune-mediated thrombotic thrombocytopenic purpuraORPHA:93585 · Frequent (79-30%)
Juvenile dermatomyositisORPHA:93672 · Frequent (79-30%)
Kidney tubulopathy-dilated cardiomyopathy syndromeORPHA:73224 · Frequent (79-30%)
LeishmaniasisORPHA:507 · Frequent (79-30%)
LeptospirosisORPHA:509 · Frequent (79-30%)
Localized sclerodermaORPHA:90289 · Frequent (79-30%)
Lowry-Wood syndromeORPHA:1824 · Frequent (79-30%)
Microscopic polyangiitisORPHA:727 · Frequent (79-30%)
Mixed connective tissue diseaseORPHA:809 · Frequent (79-30%)
Mixed-type autoimmune hemolytic anemiaORPHA:90036 · Frequent (79-30%)
Moderate hemophilia AORPHA:169805 · Frequent (79-30%)
Mucopolysaccharidosis type 1ORPHA:579 · Frequent (79-30%)
Multiple epiphyseal dysplasia-macrocephaly-facial dysmorphism syndromeORPHA:166024 · Frequent (79-30%)
Osteochondrosis of the metatarsal boneORPHA:564003 · Frequent (79-30%)
PachydermoperiostosisORPHA:2796 · Frequent (79-30%)
PAPA syndromeORPHA:69126 · Frequent (79-30%)
PFAPA syndromeORPHA:42642 · Frequent (79-30%)
PoliomyelitisORPHA:2912 · Frequent (79-30%)
Polyarteritis nodosaORPHA:767 · Frequent (79-30%)
Polycythemia veraORPHA:729 · Frequent (79-30%)
Postinfectious vasculitisORPHA:48435 · Frequent (79-30%)
Postpoliomyelitis syndromeORPHA:2942 · Frequent (79-30%)
Primary familial and congenital erythrocytosisORPHA:90042 · Frequent (79-30%)
Primary Sjögren diseaseORPHA:289390 · Frequent (79-30%)
Progressive pseudorheumatoid dysplasiaORPHA:1159 · Frequent (79-30%)
PseudoachondroplasiaORPHA:750 · Frequent (79-30%)
Psoriasis-related juvenile idiopathic arthritisORPHA:85436 · Frequent (79-30%)
Rat-bite feverORPHA:31205 · Frequent (79-30%)
Rheumatic feverORPHA:3099 · Frequent (79-30%)
Rheumatoid factor-negative polyarticular juvenile idiopathic arthritisORPHA:85408 · Frequent (79-30%)
ScleromyxedemaORPHA:167635 · Frequent (79-30%)
Silver-Russell syndromeORPHA:813 · Frequent (79-30%)
SitosterolemiaORPHA:2882 · Frequent (79-30%)
Spondyloepimetaphyseal dysplasia, Shohat typeORPHA:93352 · Frequent (79-30%)
Spondyloepiphyseal dysplasia tardaORPHA:93284 · Frequent (79-30%)
Stickler syndrome type 1ORPHA:90653 · Frequent (79-30%)
Sweet syndromeORPHA:3243 · Frequent (79-30%)
Thoracic outlet syndromeORPHA:97330 · Frequent (79-30%)
Tick-borne encephalitisORPHA:297 · Frequent (79-30%)
TularemiaORPHA:3392 · Frequent (79-30%)
TyphoidORPHA:99745 · Frequent (79-30%)
Upington diseaseORPHA:3408 · Frequent (79-30%)
Williams syndromeORPHA:904 · Frequent (79-30%)
X-linked hypophosphatemiaORPHA:89936 · Frequent (79-30%)
Yellow feverORPHA:99829 · Frequent (79-30%)
Zika virus diseaseORPHA:448237 · Frequent (79-30%)
Acquired partial lipodystrophyORPHA:79087 · Occasional (29-5%)
Acute adrenal insufficiencyORPHA:95409 · Occasional (29-5%)
Acute interstitial pneumoniaORPHA:79126 · Occasional (29-5%)
Addison diseaseORPHA:85138 · Occasional (29-5%)
African trypanosomiasisORPHA:3385 · Occasional (29-5%)
Anti-glomerular basement membrane diseaseORPHA:375 · Occasional (29-5%)
Autoerythrocyte sensitization syndromeORPHA:324636 · Occasional (29-5%)
Beta-thalassemia majorORPHA:231214 · Occasional (29-5%)
Cat-scratch diseaseORPHA:50839 · Occasional (29-5%)
Chronic graft versus host diseaseORPHA:99921 · Occasional (29-5%)
Classical Ehlers-Danlos syndromeORPHA:287 · Occasional (29-5%)
Desmoid tumorORPHA:873 · Occasional (29-5%)
Discoid lupus erythematosusORPHA:90281 · Occasional (29-5%)
Ebola hemorrhagic feverORPHA:319218 · Occasional (29-5%)
Familial cold urticariaORPHA:47045 · Occasional (29-5%)
Generalized arterial calcification of infancyORPHA:51608 · Occasional (29-5%)
Genetic hyperferritinemia without iron overloadORPHA:254704 · Occasional (29-5%)
Giant cell arteritisORPHA:397 · Occasional (29-5%)
Hereditary persistence of fetal hemoglobin-sickle cell disease syndromeORPHA:251380 · Occasional (29-5%)
Homozygous familial hypercholesterolemiaORPHA:391665 · Occasional (29-5%)
Idiopathic chronic eosinophilic pneumoniaORPHA:2902 · Occasional (29-5%)
Idiopathic hypereosinophilic syndromeORPHA:3260 · Occasional (29-5%)
Intermittent hydrarthrosisORPHA:329967 · Occasional (29-5%)
Isolated osteopoikilosisORPHA:166119 · Occasional (29-5%)
Kawasaki diseaseORPHA:2331 · Occasional (29-5%)
Kikuchi-Fujimoto diseaseORPHA:50918 · Occasional (29-5%)
Lassa feverORPHA:99824 · Occasional (29-5%)
Late-onset isolated ACTH deficiencyORPHA:199299 · Occasional (29-5%)
Legionnaires diseaseORPHA:549 · Occasional (29-5%)
ListeriosisORPHA:533 · Occasional (29-5%)
Lyme diseaseORPHA:91546 · Occasional (29-5%)
Mandibuloacral dysplasia with type A lipodystrophyORPHA:90153 · Occasional (29-5%)
Marburg hemorrhagic feverORPHA:99826 · Occasional (29-5%)
Metaphyseal chondrodysplasia, Schmid typeORPHA:174 · Occasional (29-5%)
Mosaic trisomy 3 syndromeORPHA:100071 · Occasional (29-5%)
Osteogenesis imperfectaORPHA:666 · Occasional (29-5%)
PANDASORPHA:66624 · Occasional (29-5%)
Pauci-immune glomerulonephritisORPHA:93126 · Occasional (29-5%)
Pediatric systemic lupus erythematosusORPHA:93552 · Occasional (29-5%)
PlagueORPHA:707 · Occasional (29-5%)
Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndromeORPHA:562639 · Occasional (29-5%)
Pyle diseaseORPHA:3005 · Occasional (29-5%)
Q feverORPHA:781 · Occasional (29-5%)
Recurrent infections associated with rare immunoglobulin isotypes deficiencyORPHA:183675 · Occasional (29-5%)
Refractory celiac diseaseORPHA:398063 · Occasional (29-5%)
Relapsing feverORPHA:91547 · Occasional (29-5%)
Relapsing polychondritisORPHA:728 · Occasional (29-5%)
Sagliker syndromeORPHA:300493 · Occasional (29-5%)
Severe hemophilia AORPHA:169802 · Occasional (29-5%)
Sheehan syndromeORPHA:91355 · Occasional (29-5%)
Simple cryoglobulinemiaORPHA:91139 · Occasional (29-5%)
Symptomatic form of HFE-related hemochromatosisORPHA:465508 · Occasional (29-5%)
Systemic mastocytosis with associated hematologic neoplasmORPHA:98849 · Occasional (29-5%)
Takayasu arteritisORPHA:3287 · Occasional (29-5%)
Tubulointerstitial nephritis and uveitis syndromeORPHA:91500 · Occasional (29-5%)
Tumor necrosis factor receptor 1 associated periodic syndromeORPHA:32960 · Occasional (29-5%)
Unstable beta globin chain variant diseaseORPHA:231226 · Occasional (29-5%)
Wells syndromeORPHA:901 · Occasional (29-5%)
Crimean-Congo hemorrhagic feverORPHA:99827 · Very rare (<4-1%)
Cryptogenic organizing pneumoniaORPHA:1302 · Very rare (<4-1%)
Gitelman syndromeORPHA:358 · Very rare (<4-1%)
Immune-mediated necrotizing myopathyORPHA:206569 · Very rare (<4-1%)
Isolated nail clubbingORPHA:217059 · Excluded (0%)