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- Rare systemic or rheumatologic disease ORPHA:98023
- Non-histaminic angioedema ORPHA:658
- Vasculitis ORPHA:52759
- Predominantly large-vessel vasculitis ORPHA:156140
- Juvenile temporal arteritis ORPHA:26137
- Behçet disease ORPHA:117
- Takayasu arteritis ORPHA:3287
- Giant cell arteritis ORPHA:397
- Cogan syndrome ORPHA:1467
- Hughes-Stovin syndrome ORPHA:228116
- Predominantly medium-vessel vasculitis ORPHA:156143
- Kawasaki disease ORPHA:2331
- Polyarteritis nodosa ORPHA:767
- Primary polyarteritis nodosa ORPHA:439737
- Cutaneous polyarteritis nodosa ORPHA:439729
- Single-organ polyarteritis nodosa ORPHA:439755
- Systemic polyarteritis nodosa ORPHA:439762
- Secondary polyarteritis nodosa ORPHA:439746
- Buerger disease ORPHA:36258
- Primary angiitis of the central nervous system ORPHA:140989
- Deficiency of adenosine deaminase 2 ORPHA:404553
- VEXAS syndrome ORPHA:596753
- Predominantly small-vessel vasculitis ORPHA:156146
- Primary angiitis of the central nervous system ORPHA:140989
- Anti-glomerular basement membrane disease ORPHA:375
- Immune complex mediated vasculitis ORPHA:156149
- Immunoglobulin A vasculitis ORPHA:761
- Cutaneous small vessel vasculitis ORPHA:889
- Hypocomplementemic urticarial vasculitis ORPHA:36412
- Erythema elevatum diutinum ORPHA:90000
- Cryoglobulinemic vasculitis ORPHA:91138
- Anti-neutrophil cytoplasmic antibody-associated vasculitis ORPHA:156152
- Eosinophilic granulomatosis with polyangiitis ORPHA:183
- Microscopic polyangiitis ORPHA:727
- Granulomatosis with polyangiitis ORPHA:900
- STING-associated vasculopathy with onset in infancy ORPHA:425120
- Unclassified vasculitis ORPHA:251328
- Secondary vasculitis ORPHA:445197
- Rare systemic disease ORPHA:182222
- Ehlers-Danlos/osteogenesis imperfecta syndrome ORPHA:230857
- Sepsis in premature infants ORPHA:90051
- LAMA5-related multisystemic syndrome ORPHA:521450
- Rheumatic fever ORPHA:3099
- Hereditary hemorrhagic telangiectasia ORPHA:774
- Amyloidosis ORPHA:69
- AL amyloidosis ORPHA:85443
- AA amyloidosis ORPHA:85445
- AGel amyloidosis ORPHA:85448
- Hereditary amyloidosis with primary renal involvement ORPHA:85450
- AApoAI amyloidosis ORPHA:93560
- ALys amyloidosis ORPHA:93561
- AFib amyloidosis ORPHA:93562
- AApoAII amyloidosis ORPHA:238269
- Cerebral Amyloid Angiopathy ORPHA:85458
- ABeta amyloidosis, Dutch type ORPHA:100006
- ACys amyloidosis ORPHA:100008
- ABetaL34V amyloidosis ORPHA:324703
- ABeta amyloidosis, Iowa type ORPHA:324708
- ABeta amyloidosis, Italian type ORPHA:324713
- ABetaA21G amyloidosis ORPHA:324718
- ABeta amyloidosis, Arctic type ORPHA:324723
- Hereditary ATTR amyloidosis ORPHA:271861
- Wild type ATTR amyloidosis ORPHA:330001
- ALECT2 amyloidosis ORPHA:439224
- AApoAIV amyloidosis ORPHA:439232
- ABeta2M amyloidosis ORPHA:439246
- ITM2B amyloidosis ORPHA:439254
- AH amyloidosis ORPHA:442582
- Sarcoidosis ORPHA:797
- Retinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome ORPHA:3018
- Myalgia-eosinophilia syndrome associated with tryptophan ORPHA:2582
- Langerhans cell histiocytosis ORPHA:389
- Pulmonary Langerhans cell histiocytosis ORPHA:687733
- Multisystem Langerhans cell histiocytosis ORPHA:687741
- Single-system multifocal Langerhans cell histiocytosis ORPHA:687738
- Unifocal Langerhans cell histiocytosis ORPHA:687730
- Reye syndrome ORPHA:3096
- Pyomyositis ORPHA:764
- Kimura disease ORPHA:482
- Systemic capillary leak syndrome ORPHA:188
- Hypoplasminogenemia ORPHA:722
- Kikuchi-Fujimoto disease ORPHA:50918
- Ehlers-Danlos syndrome ORPHA:98249
- Classical Ehlers-Danlos syndrome ORPHA:287
- Musculocontractural Ehlers-Danlos syndrome ORPHA:2953
- Hypermobile Ehlers-Danlos syndrome ORPHA:285
- Vascular Ehlers-Danlos syndrome ORPHA:286
- Kyphoscoliotic Ehlers-Danlos syndrome ORPHA:536545
- Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency ORPHA:1900
- Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency ORPHA:300179
- Arthrochalasia Ehlers-Danlos syndrome ORPHA:1899
- Dermatosparaxis Ehlers-Danlos syndrome ORPHA:1901
- Periodontal Ehlers-Danlos syndrome ORPHA:75392
- Spondylodysplastic Ehlers-Danlos syndrome ORPHA:536471
- B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome ORPHA:75496
- B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome ORPHA:536467
- SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome ORPHA:157965
- X-linked Ehlers-Danlos syndrome ORPHA:75497
- Brittle cornea syndrome ORPHA:90354
- Myopathic Ehlers-Danlos syndrome ORPHA:536516
- Classical-like Ehlers-Danlos syndrome type 1 ORPHA:230839
- Cardiac-valvular Ehlers-Danlos syndrome ORPHA:230851
- Classical-like Ehlers-Danlos syndrome type 2 ORPHA:536532
- Vascular Ehlers-Danlos-polymicrogyria syndrome ORPHA:636941
- Macrophage activation syndrome ORPHA:158061
- Systemic autoimmune disease ORPHA:182228
- Systemic lupus erythematosus ORPHA:536
- Familial Chilblain lupus ORPHA:481662
- Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations ORPHA:247691
- Reynolds syndrome ORPHA:779
- Relapsing polychondritis ORPHA:728
- Idiopathic inflammatory myopathy ORPHA:98482
- Immune-mediated necrotizing myopathy ORPHA:206569
- Eosinophilic fasciitis ORPHA:3165
- Antisynthetase syndrome ORPHA:81
- Focal myositis ORPHA:48918
- Inclusion body myositis ORPHA:611
- Polymyositis ORPHA:732
- Dermatomyositis ORPHA:221
- Amyopathic dermatomyositis ORPHA:645617
- Adermatopathic dermatomyositis ORPHA:645626
- Classical dermatomyositis ORPHA:645613
- Overlap myositis ORPHA:206572
- Idiopathic eosinophilic myositis ORPHA:247724
- Juvenile idiopathic inflammatory myopathy ORPHA:329888
- Juvenile dermatomyositis ORPHA:93672
- Juvenile overlap myositis ORPHA:329894
- Juvenile polymyositis ORPHA:93568
- Inflammatory myopathy with abundant macrophages ORPHA:247718
- Undifferentiated connective tissue syndrome ORPHA:90002
- Systemic sclerosis ORPHA:90291
- Diffuse cutaneous systemic sclerosis ORPHA:220393
- Limited cutaneous systemic sclerosis ORPHA:220402
- Limited systemic sclerosis ORPHA:220407
- Simple cryoglobulinemia ORPHA:91139
- Pediatric systemic lupus erythematosus ORPHA:93552
- Syndromic multisystem autoimmune disease due to Itch deficiency ORPHA:228426
- Overlapping connective tissue disease ORPHA:251312
- IgG4-related disease ORPHA:284264
- Primary cutaneous plasmacytosis ORPHA:451602
- Lymphoplasmacytic inflammatory pseudotumor of the liver ORPHA:555437
- Eosinophilic angiocentric fibrosis ORPHA:449566
- Cutaneous pseudolymphoma ORPHA:451607
- IgG4-related systemic disease ORPHA:596448
- IgG4-related retroperitoneal fibrosis ORPHA:49041
- IgG4-related mediastinitis ORPHA:63999
- IgG4-related thyroid disease ORPHA:64744
- IgG4-related dacryoadenitis and sialadenitis ORPHA:79078
- IgG4-related mesenteritis ORPHA:238593
- IgG4-related sclerosing cholangitis ORPHA:447764
- IgG4-related kidney disease ORPHA:449395
- IgG4-related aortitis ORPHA:449400
- IgG4-related pachymeningitis ORPHA:449427
- IgG4-related submandibular gland disease ORPHA:449432
- IgG4-related ophthalmic disease ORPHA:449563
- Autoimmune pancreatitis type 1 ORPHA:280302
- Autosomal systemic lupus erythematosus ORPHA:300345
- PLCG2-associated antibody deficiency and immune dysregulation ORPHA:300359
- Secondary neonatal autoimmune disease ORPHA:398091
- Transient neonatal myasthenia gravis ORPHA:391504
- Neonatal antiphospholipid syndrome ORPHA:398097
- Neonatal autoimmune hemolytic anemia ORPHA:398109
- Neonatal dermatomyositis ORPHA:398117
- Neonatal lupus erythematosus ORPHA:398124
- Neonatal scleroderma ORPHA:398127
- STAT3-related early-onset multisystem autoimmune disease ORPHA:438159
- Autoimmune interstitial lung disease-arthritis syndrome ORPHA:444092
- Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency ORPHA:444463
- Primary Sjögren syndrome ORPHA:289390
- Antiphospholipid syndrome ORPHA:80
- Satoyoshi syndrome ORPHA:3130
- Sneddon syndrome ORPHA:820
- Susac syndrome ORPHA:838
- Catastrophic antiphospholipid syndrome ORPHA:464343
- Drug-induced lupus erythematosus ORPHA:231111
- Non-Langerhans cell histiocytosis ORPHA:157987
- Rosaï-Dorfman disease ORPHA:158014
- Generalized eruptive histiocytosis ORPHA:157991
- Hereditary progressive mucinous histiocytosis ORPHA:158025
- Erdheim-Chester disease ORPHA:35687
- Multicentric reticulohistiocytosis ORPHA:139436
- Papular xanthoma ORPHA:158008
- Necrobiotic xanthogranuloma ORPHA:158011
- Xanthoma disseminatum ORPHA:158003
- Indeterminate cell histiocytosis ORPHA:158019
- Progressive nodular histiocytosis ORPHA:158022
- Benign cephalic histiocytosis ORPHA:157997
- Juvenile xanthogranuloma ORPHA:158000
- Unexplained long-lasting fever/inflammatory syndrome ORPHA:251332
- Calciphylaxis ORPHA:280062
- TEMPI syndrome ORPHA:284227
- Marfan syndrome and Marfan-related disorders ORPHA:284993
- X-linked severe syndromic thoracic aortic aneurysm and dissection ORPHA:622925
- Marfan syndrome ORPHA:558
- Isolated ectopia lentis ORPHA:1885
- Congenital contractural arachnodactyly ORPHA:115
- Shprintzen-Goldberg syndrome ORPHA:2462
- Loeys-Dietz syndrome ORPHA:60030
- Familial thoracic aortic aneurysm and aortic dissection ORPHA:91387
- Neonatal Marfan syndrome ORPHA:284979
- Aneurysm-osteoarthritis syndrome ORPHA:284984
- Cutis laxa-Marfanoid syndrome ORPHA:171719
- Connective tissue disorder due to lysyl hydroxylase-3 deficiency ORPHA:300284
- Progeroid and marfanoid aspect-lipodystrophy syndrome ORPHA:300382
- TAFRO syndrome ORPHA:457077
- Postorgasmic illness syndrome ORPHA:279947
- CAR T cell therapy-associated cytokine release syndrome ORPHA:542323
- Malignant atrophic papulosis ORPHA:679
- Familial articular hypermobility syndrome ORPHA:2295
- Multisystem inflammatory syndrome in children and adults ORPHA:598363
- Rare rheumatologic disease ORPHA:182231
- Idiopathic juvenile osteoporosis ORPHA:85193
- Juvenile idiopathic arthritis ORPHA:92
- Oligoarticular juvenile idiopathic arthritis ORPHA:85410
- Systemic-onset juvenile idiopathic arthritis ORPHA:85414
- Psoriasis-related juvenile idiopathic arthritis ORPHA:85436
- Enthesitis-related juvenile idiopathic arthritis ORPHA:85438
- Unspecified juvenile idiopathic arthritis ORPHA:91140
- Polyarticular juvenile idiopathic arthritis ORPHA:404580
- Familial calcium pyrophosphate deposition ORPHA:1416
- Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome ORPHA:2848
- Adult-onset Still disease ORPHA:829
- Reactive arthritis ORPHA:29207
- Felty syndrome ORPHA:47612
- Interstitial granulomatous dermatitis with arthritis ORPHA:79099
- Autoinflammatory syndrome ORPHA:93665
- Periodic fever syndrome ORPHA:101995
- Unexplained periodic fever syndrome ORPHA:102237
- Hereditary periodic fever syndrome ORPHA:324924
- CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome ORPHA:566067
- Infantile-onset periodic fever-panniculitis-dermatosis syndrome ORPHA:500062
- Familial Mediterranean fever ORPHA:342
- Tumor necrosis factor receptor 1 associated periodic syndrome ORPHA:32960
- NLRP3-associated autoinflammatory disease ORPHA:208650
- Muckle-Wells syndrome ORPHA:575
- CINCA syndrome ORPHA:1451
- Familial cold urticaria ORPHA:47045
- Keratitis fugax hereditaria ORPHA:647815
- NLRP12-associated hereditary periodic fever syndrome ORPHA:247868
- Mevalonate kinase deficiency ORPHA:309025
- Periodic fever-infantile enterocolitis-autoinflammatory syndrome ORPHA:436166
- NLRC4-related familial cold autoinflammatory syndrome ORPHA:576349
- Periodic fever-immunodeficiency-thrombocytopenia syndrome ORPHA:652522
- F12-associated cold autoinflammatory syndrome ORPHA:617919
- Pyogenic autoinflammatory syndrome ORPHA:324927
- Autoinflammatory syndrome with acne and/or hidradenitis suppurativa ORPHA:653434
- PAPASH syndrome ORPHA:641380
- PAPA syndrome ORPHA:69126
- PASH syndrome ORPHA:289478
- PASS syndrome ORPHA:641385
- PsAPASH syndrome ORPHA:641390
- SAPHO syndrome ORPHA:793
- Pyoderma gangrenosum ORPHA:48104
- Classic pyoderma gangrenosum ORPHA:538863
- Pustular pyoderma gangrenosum ORPHA:538866
- Bullous pyoderma gangrenosum ORPHA:538869
- Vegetative pyoderma gangrenosum ORPHA:538872
- Majeed syndrome ORPHA:77297
- Sterile multifocal osteomyelitis with periostitis and pustulosis ORPHA:210115
- Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis ORPHA:324964
- DITRA ORPHA:404546
- Hyperzincemia and hypercalprotectinemia ORPHA:251523
- Neonatal inflammatory skin and bowel disease ORPHA:294023
- Sweet syndrome ORPHA:3243
- Granulomatous autoinflammatory syndrome ORPHA:324930
- Sarcoidosis ORPHA:797
- Erdheim-Chester disease ORPHA:35687
- Blau syndrome ORPHA:90340
- Infantile onset panniculitis with uveitis and systemic granulomatosis ORPHA:251304
- Mixed autoinflammatory and autoimmune syndrome ORPHA:324933
- Early-onset autoimmunity-autoinflammation-immunodeficiency syndrome due to SOCS1 haploinsufficiency ORPHA:619948
- Early-onset immune dysregulation with autoimmunity due to DOCK11 partial deficiency ORPHA:658946
- Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation ORPHA:324530
- Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis ORPHA:329173
- PLCG2-associated antibody deficiency and immune dysregulation ORPHA:300359
- Unclassified autoinflammatory syndrome ORPHA:324936
- Behçet disease ORPHA:117
- Idiopathic recurrent pericarditis ORPHA:251307
- MAGIC syndrome ORPHA:324972
- Cherubism ORPHA:184
- Early-onset autoinflammatory syndrome due to A20 haploinsufficiency ORPHA:674762
- X-linked immune dysregulation with inflammatory bowel disease due to ELF4 deficiency ORPHA:676125
- NOCARH syndrome ORPHA:619363
- VEXAS syndrome ORPHA:596753
- Combined immunodeficiency due to RELA haploinsufficiency ORPHA:596759
- Type 1 interferonopathy ORPHA:477647
- Aicardi-Goutières syndrome ORPHA:51
- Spondyloenchondrodysplasia ORPHA:1855
- Syndromic diarrhea ORPHA:84064
- Singleton-Merten dysplasia ORPHA:85191
- X-linked reticulate pigmentary disorder ORPHA:85453
- Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations ORPHA:247691
- Autosomal systemic lupus erythematosus ORPHA:300345
- Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency ORPHA:319563
- Proteasome-associated autoinflammatory syndrome ORPHA:324977
- Deficiency of adenosine deaminase 2 ORPHA:404553
- STING-associated vasculopathy with onset in infancy ORPHA:425120
- Familial Chilblain lupus ORPHA:481662
- USP18 deficiency ORPHA:481665
- SAMD9L-associated autoinflammatory syndrome ORPHA:619367
- Intermittent hydrarthrosis ORPHA:329967
- Osteonecrosis ORPHA:399158
- Mueller-Weiss syndrome ORPHA:566943
- Epiphysiolysis of the hip ORPHA:399329
- Idiopathic phalangeal acro-osteolysis ORPHA:444316
- Osteochondritis dissecans ORPHA:2764
- Familial osteochondritis dissecans ORPHA:251262
- Avascular necrosis ORPHA:399164
- Secondary avascular necrosis ORPHA:399169
- Traumatic avascular necrosis ORPHA:399175
- Secondary non-traumatic avascular necrosis ORPHA:399180
- Rare hereditary disease with avascular necrosis ORPHA:399185
- Sickle cell anemia ORPHA:232
- Gaucher disease type 1 ORPHA:77259
- Gaucher disease type 3 ORPHA:77261
- Rare hereditary thrombophilia ORPHA:217454
- Severe hereditary thrombophilia due to congenital protein S deficiency ORPHA:743
- Severe hereditary thrombophilia due to congenital protein C deficiency ORPHA:745
- Hereditary thrombophilia due to congenital antithrombin deficiency ORPHA:82
- Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency ORPHA:217467
- Osteonecrosis of the jaw ORPHA:399293
- Primary avascular necrosis ORPHA:399302
- Osteochondrosis ORPHA:399319
- Osteochondrosis of the metatarsal bone ORPHA:564003
- Legg-Calvé-Perthes disease ORPHA:2380
- Thiemann disease, familial form ORPHA:3314
- Kienbock disease ORPHA:97332
- Osgood-Schlatter disease ORPHA:97335
- Panner disease ORPHA:97336
- Sinding-Larsen-Johansson disease ORPHA:97337
- Medial condensing osteitis of the clavicle ORPHA:57196
- Osteochondrosis of the tarsal bone ORPHA:563991
- Osteoradionecrosis of the mandible ORPHA:521127
- Fibroblastic rheumatism ORPHA:477650
- Isolated sternocostoclavicular hyperostosis ORPHA:178311
- Early-onset immune dysregulation due to DOCK11 complete deficiency ORPHA:658951
- Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome ORPHA:529977
- Rowell syndrome ORPHA:658584
- Grisel syndrome ORPHA:662255
- Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome ORPHA:238569
- Gorham-Stout disease ORPHA:73
- Hajdu-Cheney syndrome ORPHA:955