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HPO → 對應的病歷用詞，並附加具此 HPO 的疾病作為參考。
Arthritis
HP:0001369
對應病歷用詞(1)
- 關節炎權重 0.8已確認
具此 HPO 的疾病（附加參考）(122)
- Adult-onset Still diseaseORPHA:829 · Very frequent (99-80%)
- Albers-Schönberg osteopetrosisORPHA:53 · Very frequent (99-80%)
- AlkaptonuriaORPHA:56 · Very frequent (99-80%)
- Behçet diseaseORPHA:117 · Very frequent (99-80%)
- Enthesitis-related juvenile idiopathic arthritisORPHA:85438 · Very frequent (99-80%)
- Fabry diseaseORPHA:324 · Very frequent (99-80%)
- Familial calcium pyrophosphate depositionORPHA:1416 · Very frequent (99-80%)
- Familial cold urticariaORPHA:47045 · Very frequent (99-80%)
- Farber diseaseORPHA:333 · Very frequent (99-80%)
- Felty syndromeORPHA:47612 · Very frequent (99-80%)
- Mixed connective tissue diseaseORPHA:809 · Very frequent (99-80%)
- Muckle-Wells syndromeORPHA:575 · Very frequent (99-80%)
- Multicentric osteolysis-nodulosis-arthropathy spectrumORPHA:371428 · Very frequent (99-80%)
- Multicentric reticulohistiocytosisORPHA:139436 · Very frequent (99-80%)
- Oligoarticular juvenile idiopathic arthritisORPHA:85410 · Very frequent (99-80%)
- PAPA syndromeORPHA:69126 · Very frequent (99-80%)
- Reactive arthritisORPHA:29207 · Very frequent (99-80%)
- Relapsing polychondritisORPHA:728 · Very frequent (99-80%)
- Rheumatic feverORPHA:3099 · Very frequent (99-80%)
- Rheumatoid factor-positive polyarticular juvenile idiopathic arthritisORPHA:85435 · Very frequent (99-80%)
- Schnitzler syndromeORPHA:37748 · Very frequent (99-80%)
- Systemic-onset juvenile idiopathic arthritisORPHA:85414 · Very frequent (99-80%)
- Whipple diseaseORPHA:3452 · Very frequent (99-80%)
- Wild type ABeta2M amyloidosisORPHA:85446 · Very frequent (99-80%)
- Wilson diseaseORPHA:905 · Very frequent (99-80%)
- Antisynthetase syndromeORPHA:81 · Frequent (79-30%)
- Autosomal non-syndromic agammaglobulinemiaORPHA:33110 · Frequent (79-30%)
- Blau syndromeORPHA:90340 · Frequent (79-30%)
- BrucellosisORPHA:1304 · Frequent (79-30%)
- ChikungunyaORPHA:324625 · Frequent (79-30%)
- Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitisORPHA:324964 · Frequent (79-30%)
- Combined immunodeficiency with facio-oculo-skeletal anomaliesORPHA:221139 · Frequent (79-30%)
- Cranio-osteoarthropathyORPHA:1525 · Frequent (79-30%)
- Cryoglobulinemic vasculitisORPHA:91138 · Frequent (79-30%)
- DermatomyositisORPHA:221 · Frequent (79-30%)
- Diffuse cutaneous systemic sclerosisORPHA:220393 · Frequent (79-30%)
- DracunculiasisORPHA:231 · Frequent (79-30%)
- Eng-Strom syndromeORPHA:1937 · Frequent (79-30%)
- Eosinophilic fasciitisORPHA:3165 · Frequent (79-30%)
- Familial Mediterranean feverORPHA:342 · Frequent (79-30%)
- Generalized pustular psoriasisORPHA:247353 · Frequent (79-30%)
- Giant cell arteritisORPHA:397 · Frequent (79-30%)
- Granulomatosis with polyangiitisORPHA:900 · Frequent (79-30%)
- Hyperimmunoglobulinemia D with periodic feverORPHA:343 · Frequent (79-30%)
- Hypocomplementemic urticarial vasculitisORPHA:36412 · Frequent (79-30%)
- Immunoglobulin A vasculitisORPHA:761 · Frequent (79-30%)
- Juvenile dermatomyositisORPHA:93672 · Frequent (79-30%)
- Kawasaki diseaseORPHA:2331 · Frequent (79-30%)
- Lyme diseaseORPHA:91546 · Frequent (79-30%)
- Mild phosphoribosylpyrophosphate synthetase superactivityORPHA:411536 · Frequent (79-30%)
- Myalgia-eosinophilia syndrome associated with tryptophanORPHA:2582 · Frequent (79-30%)
- Nail-patella syndromeORPHA:2614 · Frequent (79-30%)
- Oculocerebrorenal syndrome of LoweORPHA:534 · Frequent (79-30%)
- Osteochondrosis of the metatarsal boneORPHA:564003 · Frequent (79-30%)
- Overlap myositisORPHA:206572 · Frequent (79-30%)
- PachydermoperiostosisORPHA:2796 · Frequent (79-30%)
- PolymyositisORPHA:732 · Frequent (79-30%)
- Psoriasis-related juvenile idiopathic arthritisORPHA:85436 · Frequent (79-30%)
- Rat-bite feverORPHA:31205 · Frequent (79-30%)
- Reynolds syndromeORPHA:779 · Frequent (79-30%)
- Rheumatoid factor-negative polyarticular juvenile idiopathic arthritisORPHA:85408 · Frequent (79-30%)
- SAPHO syndromeORPHA:793 · Frequent (79-30%)
- Severe phosphoribosylpyrophosphate synthetase superactivityORPHA:411543 · Frequent (79-30%)
- Systemic lupus erythematosusORPHA:536 · Frequent (79-30%)
- Takayasu arteritisORPHA:3287 · Frequent (79-30%)
- Tenosynovial giant cell tumorORPHA:66627 · Frequent (79-30%)
- Tumor necrosis factor receptor 1 associated periodic syndromeORPHA:32960 · Frequent (79-30%)
- X-linked agammaglobulinemiaORPHA:47 · Frequent (79-30%)
- Zika virus diseaseORPHA:448237 · Frequent (79-30%)
- 22q11.2 deletion syndromeORPHA:567 · Occasional (29-5%)
- Activated PI3K-delta syndromeORPHA:397596 · Occasional (29-5%)
- Adiposis dolorosaORPHA:36397 · Occasional (29-5%)
- Aicardi-Goutières syndromeORPHA:51 · Occasional (29-5%)
- Alpha-mannosidosisORPHA:61 · Occasional (29-5%)
- Anti-glomerular basement membrane diseaseORPHA:375 · Occasional (29-5%)
- AspartylglucosaminuriaORPHA:93 · Occasional (29-5%)
- Autoimmune hepatitisORPHA:2137 · Occasional (29-5%)
- Autosomal dominant spastic paraplegia type 36ORPHA:320365 · Occasional (29-5%)
- Bacterial toxic-shock syndromeORPHA:36234 · Occasional (29-5%)
- Cat-scratch diseaseORPHA:50839 · Occasional (29-5%)
- Catastrophic antiphospholipid syndromeORPHA:464343 · Occasional (29-5%)
- ChoreoacanthocytosisORPHA:2388 · Occasional (29-5%)
- Chronic graft versus host diseaseORPHA:99921 · Occasional (29-5%)
- CoccidioidomycosisORPHA:228123 · Occasional (29-5%)
- Congenital atransferrinemiaORPHA:1195 · Occasional (29-5%)
- Congenital tufting enteropathyORPHA:92050 · Occasional (29-5%)
- Eosinophilic granulomatosis with polyangiitisORPHA:183 · Occasional (29-5%)
- Graft versus host diseaseORPHA:39812 · Occasional (29-5%)
- HNF1B-related autosomal dominant tubulointerstitial kidney diseaseORPHA:93111 · Occasional (29-5%)
- Idiopathic hypereosinophilic syndromeORPHA:3260 · Occasional (29-5%)
- Idiopathic non-lupus full-house nephropathyORPHA:567544 · Occasional (29-5%)
- KID syndromeORPHA:477 · Occasional (29-5%)
- Localized sclerodermaORPHA:90289 · Occasional (29-5%)
- MelorheostosisORPHA:2485 · Occasional (29-5%)
- Microscopic polyangiitisORPHA:727 · Occasional (29-5%)
- Mueller-Weiss syndromeORPHA:566943 · Occasional (29-5%)
- Multiple osteochondromasORPHA:321 · Occasional (29-5%)
- Non-syndromic agammaglobulinemiaORPHA:229717 · Occasional (29-5%)
- Osteochondrosis of the tarsal boneORPHA:563991 · Occasional (29-5%)
- Pediatric systemic lupus erythematosusORPHA:93552 · Occasional (29-5%)
- PFAPA syndromeORPHA:42642 · Occasional (29-5%)
- Postinfectious vasculitisORPHA:48435 · Occasional (29-5%)
- Primary Sjögren diseaseORPHA:289390 · Occasional (29-5%)
- Recurrent infections associated with rare immunoglobulin isotypes deficiencyORPHA:183675 · Occasional (29-5%)
- RIDDLE syndromeORPHA:420741 · Occasional (29-5%)
- SarcoidosisORPHA:797 · Occasional (29-5%)
- Simple cryoglobulinemiaORPHA:91139 · Occasional (29-5%)
- SpondyloenchondrodysplasiaORPHA:1855 · Occasional (29-5%)
- Symptomatic form of HFE-related hemochromatosisORPHA:465508 · Occasional (29-5%)
- Systemic sclerosisORPHA:90291 · Occasional (29-5%)
- Tetrasomy 9p syndromeORPHA:3310 · Occasional (29-5%)
- Wiskott-Aldrich syndromeORPHA:906 · Occasional (29-5%)
- X-linked hypophosphatemiaORPHA:89936 · Occasional (29-5%)
- X-linked lymphoproliferative disease due to XIAP deficiencyORPHA:538934 · Occasional (29-5%)
- Autoimmune lymphoproliferative syndromeORPHA:3261 · Very rare (<4-1%)
- Dowling-Degos diseaseORPHA:79145 · Very rare (<4-1%)
- FusariosisORPHA:228119 · Very rare (<4-1%)
- Lacrimoauriculodentodigital syndromeORPHA:2363 · Very rare (<4-1%)
- Marburg hemorrhagic feverORPHA:99826 · Very rare (<4-1%)
- MYH14-related peripheral neuropathy-myopathy-hoarseness-hearing loss syndromeORPHA:397744 · Very rare (<4-1%)
- PlagueORPHA:707 · Very rare (<4-1%)
- ShigellosisORPHA:810 · Very rare (<4-1%)