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- Rare circulatory system disease ORPHA:98028
- Rare vascular disease ORPHA:68362
- Non-inflammatory vasculopathy ORPHA:496924
- May-Thurner syndrome ORPHA:675404
- Neonatal compartment syndrome ORPHA:641829
- Segmental arterial mediolysis ORPHA:645350
- Isolated spontaneous cervical artery dissection ORPHA:689001
- Fibromuscular dysplasia ORPHA:698012
- Fibromuscular dysplasia of the cervical and intracranial arteries ORPHA:698036
- Fibromuscular dysplasia of the renal arteries ORPHA:698043
- Fibromuscular dysplasia of the coronary arteries ORPHA:698059
- Fibromuscular dysplasia of the visceral arteries ORPHA:698063
- Fibromuscular dysplasia of the arteries of the extremities ORPHA:698069
- Fontan-associated liver disease ORPHA:699068
- Acute peripheral arterial occlusion ORPHA:90064
- Livedoid vasculopathy ORPHA:542643
- Secondary erythromelalgia ORPHA:529864
- Arterial dissection-lentiginosis syndrome ORPHA:1682
- Sneddon syndrome ORPHA:820
- Rare genetic vascular disease ORPHA:233655
- Familial abdominal aortic aneurysm ORPHA:86
- Generalized arterial calcification of infancy ORPHA:51608
- Rare disease with thoracic aortic aneurysm and aortic dissection ORPHA:285014
- X-linked severe syndromic thoracic aortic aneurysm and dissection ORPHA:622925
- Marfan syndrome ORPHA:558
- Arterial tortuosity syndrome ORPHA:3342
- Vascular Ehlers-Danlos syndrome ORPHA:286
- Loeys-Dietz syndrome ORPHA:60030
- Familial thoracic aortic aneurysm and aortic dissection ORPHA:91387
- Neonatal Marfan syndrome ORPHA:284979
- Aneurysm-osteoarthritis syndrome ORPHA:284984
- Familial bicuspid aortic valve ORPHA:402075
- Multisystemic smooth muscle dysfunction syndrome ORPHA:404463
- Familial aortic dissection ORPHA:229
- Hereditary arterial and articular multiple calcification syndrome ORPHA:289601
- Lethal arteriopathy syndrome due to fibulin-4 deficiency ORPHA:314718
- Autosomal recessive cutis laxa type 1 ORPHA:90349
- Calciphylaxis ORPHA:280062
- Pediatric arterial ischemic stroke ORPHA:439175
- Susac syndrome ORPHA:838
- 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 vascular anomaly ORPHA:68419
- Fast-flow vascular malformation ORPHA:211266
- Unifocal fast-flow vascular malformation ORPHA:715762
- Peripheral fast-flow vascular malformation ORPHA:707944
- Peripheral congenital arteriovenous fistula ORPHA:708051
- Intramuscular fast-flow vascular anomaly ORPHA:708007
- Peripheral arteriovenous malformation ORPHA:708046
- Fast-flow vascular malformation of the central nervous system ORPHA:715744
- Intracranial fast-flow vascular malformation ORPHA:715750
- Brain arteriovenous malformation ORPHA:46724
- Brain pial arteriovenous fistula ORPHA:715292
- Acquired intracranial dural arteriovenous fistula ORPHA:715318
- Dural sinus malformation with arteriovenous shunt ORPHA:97339
- Cerebral proliferative angiopathy ORPHA:692271
- Vein of Galen malformation ORPHA:1053
- Spinal fast-flow vascular malformation ORPHA:715025
- Metameric fast-flow vascular malformation ORPHA:715757
- Spinal arteriovenous metameric syndrome ORPHA:53721
- Cerebrofacial arteriovenous metameric syndrome ORPHA:141189
- Visceral arteriovenous malformation ORPHA:693855
- Hepatic arteriovenous malformation ORPHA:693846
- Renal arteriovenous malformation ORPHA:693839
- Gastrointestinal tract arteriovenous malformation ORPHA:693832
- Splenic arteriovenous malformation ORPHA:693863
- Uterine arteriovenous malformation ORPHA:693815
- Pancreatic arteriovenous malformation ORPHA:693826
- Gallblader arteriovenous malformation ORPHA:693869
- Urinary tract arteriovenous malformation ORPHA:693872
- Pulmonary arteriovenous malformation ORPHA:2038
- Arteriovenous malformation of the thoraco-abdominal-pelvic cavity ORPHA:714698
- Capillary malformation-arteriovenous malformation ORPHA:137667
- RASA1-related capillary malformation-arteriovenous malformation ORPHA:693907
- EPHB4-related capillary malformation-arteriovenous malformation ORPHA:693912
- Hereditary hemorrhagic telangiectasia ORPHA:774
- Parkes Weber syndrome ORPHA:90307
- Slow-flow malformation, venous type ORPHA:211252
- Multifocal peripheral venous malformation ORPHA:715339
- Mucocutaneous venous malformations ORPHA:2451
- Multifocal sporadic venous malformation ORPHA:714806
- Glomuvenous malformation ORPHA:83454
- Familial intraosseous vascular malformation ORPHA:140436
- Blue rubber bleb nevus ORPHA:1059
- Unifocal peripheral venous malformation ORPHA:715334
- Unifocal sporadic venous malformation ORPHA:714785
- Intraosseous venous malformation ORPHA:715923
- Verrucous hemangioma ORPHA:464318
- Fibro-adipose vascular anomaly ORPHA:699683
- Splenic venous malformation ORPHA:688523
- Segmental venous malformation ORPHA:217008
- Glomuvenous malformation ORPHA:83454
- Dural sinus malformation without arteriovenous shunt ORPHA:717564
- CLOVES syndrome ORPHA:140944
- Maffucci syndrome ORPHA:163634
- Sinus pericranii ORPHA:714734
- Familial cerebral cavernous malformation ORPHA:221061
- Capillary-lymphatic-venous malformation with segmental distribution ORPHA:90308
- Rare capillary malformation ORPHA:211247
- Angioma serpiginosum ORPHA:95429
- Phakomatosis pigmentovascularis ORPHA:2875
- Phakomatosis cesioflammea ORPHA:79483
- Phakomatosis cesiomarmorata ORPHA:79484
- Phakomatosis spilorosea ORPHA:79485
- Microcephaly-capillary malformation syndrome ORPHA:294016
- Familial multiple nevi flammei ORPHA:624
- Diffuse capillary malformation with overgrowth ORPHA:714737
- Rare capillary malformation with associated anomalies ORPHA:458830
- Port-wine nevi-mega cisterna magna-hydrocephalus syndrome ORPHA:2703
- Hemihyperplasia-multiple lipomatosis syndrome ORPHA:276280
- Geographic pattern capillary malformation ORPHA:715446
- Isolated geographic pattern capillary malformation ORPHA:715345
- Syndromic geographic pattern capillary malformation ORPHA:715460
- Reticulated capillary malformation ORPHA:715453
- Isolated reticulated capillary malformation ORPHA:715353
- Megalencephaly-capillary malformation-polymicrogyria syndrome ORPHA:60040
- Diffuse capillary malformation with overgrowth ORPHA:714737
- Low resistance capillary malformation ORPHA:715463
- Isolated low resistance capillary malformation ORPHA:715359
- Syndromic low resistance capillary malformation ORPHA:715466
- Sturge-Weber syndrome ORPHA:3205
- Cutis marmorata telangiectatica congenita ORPHA:1556
- Slow-flow malformation, lymphatic type ORPHA:211255
- Primary lymphedema ORPHA:77240
- Primary lymphedema without systemic or visceral involvement ORPHA:568041
- Congenital primary lymphedema without systemic or visceral involvement ORPHA:2416
- Amniotic band syndrome ORPHA:295000
- Milroy disease ORPHA:79452
- Congenital primary lymphedema of Gordon ORPHA:569821
- Microcephaly-lymphedema-chorioretinopathy syndrome ORPHA:2526
- German syndrome ORPHA:2077
- Late-onset primary lymphedema without systemic or visceral involvement ORPHA:289825
- Primary lymphedema with systemic or visceral involvement ORPHA:568044
- Dahlberg-Borer-Newcomer syndrome ORPHA:1563
- Aplasia cutis congenita-intestinal lymphangiectasia syndrome ORPHA:1116
- Hennekam syndrome ORPHA:2136
- EPHB4-related lymphatic-related hydrops fetalis ORPHA:568065
- PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis ORPHA:568062
- Warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome ORPHA:568056
- Lymphedema with yellow nails ORPHA:662
- Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome ORPHA:69735
- Lymphedema-atrial septal defects-facial changes syndrome ORPHA:86915
- Disorder with multisystemic involvement and primary lymphedema ORPHA:568047
- Takenouchi-Kosaki syndrome ORPHA:487796
- Fabry disease ORPHA:324
- Noonan syndrome ORPHA:648
- Turner syndrome ORPHA:881
- Monosomy X syndrome ORPHA:99226
- Mosaic monosomy X syndrome ORPHA:99228
- Turner syndrome due to structural X chromosome anomalies ORPHA:99413
- Cardiofaciocutaneous syndrome ORPHA:1340
- Müllerian derivatives-lymphangiectasia-polydactyly syndrome ORPHA:1655
- PEHO syndrome ORPHA:2836
- Phelan-McDermid syndrome ORPHA:48652
- Phelan-McDermid syndrome due to SHANK3 mutation ORPHA:662172
- Phelan-McDermid syndrome due to 22q13.3 deletion ORPHA:662169
- Hypohidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome ORPHA:69088
- Oculodentodigital dysplasia ORPHA:2710
- PEHO-like syndrome ORPHA:99807
- Tuberous sclerosis complex ORPHA:805
- Prolidase deficiency ORPHA:742
- Isolated rare lymphatic malformation ORPHA:2415
- Lymphedema-posterior choanal atresia syndrome ORPHA:99141
- Common cystic lymphatic malformation ORPHA:458833
- Macrocystic lymphatic malformation ORPHA:79489
- Microcystic lymphatic malformation ORPHA:79490
- Mixed cystic lymphatic malformation ORPHA:458792
- Diffuse lymphatic malformation ORPHA:141209
- Gorham-Stout disease ORPHA:73
- Kaposiform lymphangiomatosis ORPHA:464329
- Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome ORPHA:464321
- Coagulation abnormality associated with a vascular anomaly ORPHA:717582
- Kasabach-Merritt phenomenon ORPHA:2330
- Kasabach-Merritt-like phenomenon ORPHA:717585
- Localized intravascular coagulation ORPHA:717588
- Disseminated intravascular coagulation associated with a vascular anomaly ORPHA:717593
- Complex vascular malformation with associated anomalies ORPHA:211277
- Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome ORPHA:137608
- Bannayan-Riley-Ruvalcaba syndrome ORPHA:109
- Lymphedema-cerebral arteriovenous anomaly-primary pulmonary hypertension syndrome ORPHA:86914
- Proteus syndrome ORPHA:744
- Rare combined vascular malformation ORPHA:458837
- Capillary-venous malformation ORPHA:717611
- Capillary-lymphatic malformation ORPHA:717605
- Lymphatic-venous malformation ORPHA:717598
- Capillary-lymphatic-venous malformation ORPHA:717619
- Verrucous hemangioma ORPHA:464318
- Rare vascular malformation of major vessels ORPHA:458844
- Internal carotid absence ORPHA:981
- Congenital anomaly of the great arteries ORPHA:98724
- Aortic arch defects ORPHA:1132
- Encircling double aortic arch ORPHA:99075
- Persistent fifth aortic arch ORPHA:99076
- Kommerell diverticulum ORPHA:99077
- Neuhauser anomaly ORPHA:99078
- Cervical aortic arch ORPHA:99079
- Right aortic arch ORPHA:99081
- Dysphagia lusoria ORPHA:99082
- Scimitar syndrome ORPHA:185
- Arterial duct anomaly ORPHA:95485
- Premature closure of the arterial duct ORPHA:95486
- Congenital patent ductus arteriosus aneurysm ORPHA:99072
- Familial patent arterial duct ORPHA:466729
- Aortic malformation ORPHA:98718
- Supravalvular aortic stenosis ORPHA:3193
- Middle aortic syndrome ORPHA:1456
- Quadricuspid aortic valve ORPHA:542568
- Coarctation of aorta ORPHA:1457
- Aortic arch interruption ORPHA:2299
- Fixed subaortic stenosis ORPHA:3092
- Discrete fixed membranous subaortic stenosis ORPHA:99051
- Discrete fibromuscular subaortic stenosis ORPHA:99052
- Tunnel subaortic stenosis ORPHA:99053
- Congenital aortic valve stenosis ORPHA:3093
- Familial bicuspid aortic valve ORPHA:402075
- Pulmonary artery or pulmonary branch anomaly ORPHA:98719
- Pulmonary atresia-intact ventricular septum syndrome ORPHA:1208
- Pulmonary valve agenesis ORPHA:982
- Pulmonary valve agenesis-intact ventricular septum-persistent ductus arteriosus syndrome ORPHA:99048
- Pulmonary valve agenesis-tetralogy of Fallot-absence of ductus arteriosus syndrome ORPHA:101206
- Absence of the pulmonary artery ORPHA:980
- Congenital pulmonary valvar stenosis ORPHA:3189
- Subpulmonary stenosis ORPHA:3190
- Supravalvular pulmonary stenosis ORPHA:3192
- Valvular pulmonary stenosis ORPHA:99054
- Idiopathic pulmonary artery dilatation ORPHA:1676
- Pulmonary artery hypoplasia ORPHA:99083
- Peripheral pulmonary stenosis ORPHA:99084
- Ascending aorta anomaly ORPHA:98725
- Congenital anomaly of the great veins ORPHA:363189
- Congenital systemic veins anomaly ORPHA:3091
- Congenital anomaly of superior vena cava ORPHA:95498
- Right superior vena cava connecting to left-sided atrium ORPHA:99110
- Primary superior vena cava aneurysm ORPHA:652668
- Agenesis of the superior vena cava ORPHA:99114
- Persistent left superior vena cava connecting to the roof of left-sided atrium ORPHA:99111
- Subaortic course of innominate vein ORPHA:99113
- Persistent left superior vena cava connecting through coronary sinus to left-sided atrium ORPHA:99109
- Absence of innominate vein ORPHA:99112
- Congenital anomaly of the inferior vena cava ORPHA:95499
- Right inferior vena cava connecting to left-sided atrium ORPHA:99119
- Persistent eustachian valve ORPHA:99120
- Congenital stenosis of the inferior vena cava ORPHA:99122
- Inferior vena cava interruption without azygos continuation ORPHA:99123
- Primary inferior vena cava aneurysm ORPHA:652678
- Azygos continuation of the inferior vena cava ORPHA:99121
- Congenital anomaly of the coronary sinus ORPHA:95500
- Congenital anomaly of hepatic vein ORPHA:95507
- Congenital portosystemic shunt ORPHA:480531
- Congenital pulmonary veins anomaly ORPHA:98729
- Congenital renal artery stenosis ORPHA:97598
- Carotid web ORPHA:698260
- Extracranial carotid artery aneurysm ORPHA:494424
- Rare vascular tumor ORPHA:211237
- Malignant vascular tumor ORPHA:673466
- Benign vascular tumor ORPHA:673470
- Circumscribed choroidal hemangioma ORPHA:714138
- Hereditary neurocutaneous malformation ORPHA:1062
- Tufted angioma ORPHA:1063
- Retinal capillary malformation ORPHA:71213
- Spindle cell hemangioma ORPHA:210584
- Congenital hemangioma ORPHA:458775
- Rapidly involuting congenital hemangioma ORPHA:141184
- Partially involuting congenital hemangioma ORPHA:458785
- Non-involuting congenital hemangioma ORPHA:141179
- Anastomosing haemangioma ORPHA:675359
- Acquired elastotic haemangioma ORPHA:675597
- Hobnail hemangioma ORPHA:675362
- Microvenular haemangioma ORPHA:675369
- Epithelioid hemangioma ORPHA:675396
- Papillary hemangioma ORPHA:673543
- Reactive angioendotheliomatosis ORPHA:673574
- Eccrine angiomatous hamartoma ORPHA:673568
- Littoral cell hemangioma of the spleen ORPHA:673538
- Intravascular papillary endothelial hyperplasia ORPHA:673525
- Rare infantile hemangioma ORPHA:210589
- Borderline vascular tumor ORPHA:673473
- Simple vascular malformation ORPHA:211243