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- Rare respiratory disease ORPHA:97955
- Mounier-Kühn syndrome ORPHA:3347
- Pulmonary alveolar microlithiasis ORPHA:60025
- IgG4-related mediastinitis ORPHA:63999
- Rare pulmonary hypertension ORPHA:71198
- Chronic thromboembolic pulmonary hypertension ORPHA:70591
- Pulmonary arterial hypertension ORPHA:182090
- Idiopathic/heritable pulmonary arterial hypertension ORPHA:422
- Idiopathic pulmonary arterial hypertension ORPHA:275766
- Heritable pulmonary arterial hypertension ORPHA:275777
- Drug- or toxin-induced pulmonary arterial hypertension ORPHA:275786
- Pulmonary arterial hypertension associated with another disease ORPHA:275791
- Pulmonary arterial hypertension associated with connective tissue disease ORPHA:275798
- Pulmonary arterial hypertension associated with congenital heart disease ORPHA:275803
- Pulmonary arterial hypertension associated with HIV infection ORPHA:275808
- Pulmonary arterial hypertension associated with portal hypertension ORPHA:275813
- Pulmonary arterial hypertension associated with schistosomiasis ORPHA:275823
- Pulmonary arterial hypertension associated with chronic hemolytic anemia ORPHA:275828
- Pulmonary hypertension owing to lung disease and/or hypoxia ORPHA:275837
- Pulmonary hypertension with unclear multifactorial mechanism ORPHA:275844
- Syndrome with pulmonary hypertension as a major feature ORPHA:275853
- Braddock syndrome ORPHA:52047
- Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome ORPHA:363694
- Multisystemic smooth muscle dysfunction syndrome ORPHA:404463
- Pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis ORPHA:431353
- Respiratory or thoracic malformation ORPHA:97957
- Thoracic malformation ORPHA:182108
- Short rib-polydactyly syndrome ORPHA:1505
- Jeune syndrome ORPHA:474
- Ellis Van Creveld syndrome ORPHA:289
- Cranioectodermal dysplasia ORPHA:1515
- Short rib-polydactyly syndrome, Beemer-Langer type ORPHA:93268
- Short rib-polydactyly syndrome, Majewski type ORPHA:93269
- Short rib-polydactyly syndrome, Saldino-Noonan type ORPHA:93270
- Short rib-polydactyly syndrome, Verma-Naumoff type ORPHA:93271
- Joubert syndrome with Jeune asphyxiating thoracic dystrophy ORPHA:397715
- Short rib-polydactyly syndrome type 5 ORPHA:498497
- Acropectorovertebral dysplasia ORPHA:957
- Fetal akinesia deformation sequence ORPHA:994
- Lethal congenital contracture syndrome type 1 ORPHA:1486
- Thoracomelic dysplasia ORPHA:1803
- Thoracic dysplasia-hydrocephalus syndrome ORPHA:1861
- Sternal cleft ORPHA:2017
- Congenitally short costocoracoid ligament ORPHA:2391
- Matthew-Wood syndrome ORPHA:2470
- Orofaciodigital syndrome type 4 ORPHA:2753
- Sprengel deformity ORPHA:3181
- Thoracolaryngopelvic dysplasia ORPHA:3317
- Ossification anomalies-psychomotor developmental delay syndrome ORPHA:73230
- NEK9-related lethal skeletal dysplasia ORPHA:464366
- Respiratory malformation ORPHA:182111
- Pulmonary artery hypoplasia ORPHA:99083
- Congenital pulmonary veins atresia or stenosis ORPHA:3188
- Scimitar syndrome ORPHA:185
- Congenital pulmonary lymphangiectasia ORPHA:2414
- Congenital pulmonary airway malformation ORPHA:2444
- Congenital pulmonary airway malformation type 0 ORPHA:280827
- Congenital pulmonary airway malformation type 1 ORPHA:280832
- Congenital pulmonary airway malformation type 2 ORPHA:280840
- Congenital pulmonary airway malformation type 3 ORPHA:280847
- Congenital pulmonary airway malformation type 4 ORPHA:280854
- Tracheal agenesis ORPHA:3346
- Pulmonary agenesis ORPHA:984
- Congenital respiratory-biliary fistula ORPHA:2040
- Congenital lobar emphysema ORPHA:1928
- Lung agenesis-heart defect-thumb anomalies syndrome ORPHA:1120
- Laryngotracheoesophageal cleft ORPHA:2004
- Laryngotracheoesophageal cleft type 1 ORPHA:93938
- Laryngotracheoesophageal cleft type 2 ORPHA:93939
- Laryngotracheoesophageal cleft type 3 ORPHA:93940
- Laryngotracheoesophageal cleft type 4 ORPHA:93941
- Laryngotracheoesophageal cleft type 0 ORPHA:280205
- Primary pulmonary hypoplasia ORPHA:2257
- Laryngo-onycho-cutaneous syndrome ORPHA:2407
- Matthew-Wood syndrome ORPHA:2470
- Growth delay-hydrocephaly-lung hypoplasia syndrome ORPHA:3035
- Thoracolaryngopelvic dysplasia ORPHA:3317
- 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
- Congenital pulmonary sequestration ORPHA:3161
- Intralobar congenital pulmonary sequestration ORPHA:280802
- Extralobar congenital pulmonary sequestration ORPHA:280811
- Communicating congenital bronchopulmonary-foregut malformation ORPHA:280821
- Bronchopulmonary dysplasia ORPHA:70589
- Congenital tracheomalacia ORPHA:95430
- Williams-Campbell syndrome ORPHA:411501
- Bronchial malformation ORPHA:649014
- Non-syndromic bridging bronchus ORPHA:648992
- Non-syndromic congenital bronchial atresia ORPHA:649010
- Isolated left bronchial isomerism ORPHA:649029
- Bronchogenic cyst ORPHA:2357
- Hereditary hemorrhagic telangiectasia ORPHA:774
- Isolated tracheoesophageal fistula ORPHA:454750
- Pulmonary arteriovenous malformation ORPHA:2038
- Abnormal origin of right or left pulmonary artery from the aorta ORPHA:99050
- Rare respiratory tumor ORPHA:98060
- SMARCA4-deficient sarcoma of thorax ORPHA:466962
- Nasopharyngeal carcinoma ORPHA:150
- Rare bronchopulmonary and pleural cavity tumors ORPHA:101945
- Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia ORPHA:617916
- Primary pulmonary lymphoma ORPHA:2420
- Pleural mesothelioma ORPHA:50251
- Diffused pleural mesothelioma ORPHA:675837
- Localized pleural mesothelioma ORPHA:675833
- Pleural mesothelioma in situ ORPHA:675841
- Pulmonary blastoma ORPHA:64741
- Pleuropulmonary blastoma ORPHA:64742
- Pleuropulmonary blastoma type 1 ORPHA:99933
- Pleuropulmonary blastoma type 2 ORPHA:99934
- Pleuropulmonary blastoma type 3 ORPHA:99935
- DICER1 tumor-predisposition syndrome ORPHA:284343
- Fetal lung interstitial tumor ORPHA:284362
- Small cell lung cancer ORPHA:70573
- Bronchial neuroendocrine tumor ORPHA:97287
- Well-differentiated fetal adenocarcinoma of the lung ORPHA:284395
- Well-differentiated papillary mesothelial tumour of the pleura ORPHA:675822
- Adenomatoid tumour of the pleura ORPHA:675814
- Rare pulmonary disease ORPHA:101944
- 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
- Cystic fibrosis ORPHA:586
- Alpha-1-antitrypsin deficiency ORPHA:60
- Congenital diaphragmatic hernia ORPHA:2140
- Familial spontaneous pneumothorax ORPHA:2903
- Primary ciliary dyskinesia ORPHA:244
- Allergic bronchopulmonary aspergillosis ORPHA:1164
- Young syndrome ORPHA:3471
- Siegler-Brewer-Carey syndrome ORPHA:3167
- Bronchiolitis obliterans ORPHA:1303
- Transplant-related bronchiolitis obliterans ORPHA:658602
- Non-transplant-related bronchiolitis obliterans ORPHA:658612
- Tracheobronchopathia osteochondroplastica ORPHA:3348
- Staphylococcal necrotizing pneumonia ORPHA:36238
- Pulmonary nodular lymphoid hyperplasia ORPHA:60026
- Recurrent respiratory papillomatosis ORPHA:60032
- Idiopathic bronchiectasis ORPHA:60033
- Meconium aspiration syndrome ORPHA:70588
- Infantile apnea ORPHA:70590
- Diffuse alveolar hemorrhage ORPHA:90060
- Systemic sclerosis ORPHA:90291
- Diffuse cutaneous systemic sclerosis ORPHA:220393
- Limited cutaneous systemic sclerosis ORPHA:220402
- Limited systemic sclerosis ORPHA:220407
- Pulmonary arteriovenous malformation ORPHA:2038
- Severe acute respiratory syndrome ORPHA:140896
- Sudden infant death-dysgenesis of the testes syndrome ORPHA:168593
- Diffuse panbronchiolitis ORPHA:171700
- Acute lung injury ORPHA:178320
- Interstitial lung disease ORPHA:182095
- Interstitial lung disease specific to childhood ORPHA:264656
- Primary interstitial lung disease specific to childhood ORPHA:264665
- Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome ORPHA:137631
- Primary interstitial lung disease specific to childhood due to alveolar structure disorder ORPHA:264670
- Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies ORPHA:100049
- Brain-lung-thyroid syndrome ORPHA:209905
- Neonatal acute respiratory distress syndrome ORPHA:217563
- Hereditary pulmonary alveolar proteinosis ORPHA:264675
- Interstitial lung disease due to ABCA3 deficiency ORPHA:440402
- Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency ORPHA:440427
- Infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia ORPHA:572428
- Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome ORPHA:306504
- Primary interstitial lung disease specific to childhood due to alveolar vascular disorder ORPHA:264683
- Congenital pulmonary lymphangiectasia ORPHA:2414
- Lymphedema with yellow nails ORPHA:662
- Congenital alveolar capillary dysplasia ORPHA:210122
- Congenital chylothorax ORPHA:264688
- Isolated pulmonary capillaritis ORPHA:264691
- 16q24.1 microdeletion syndrome ORPHA:352629
- Interstitial lung disease specific to infancy ORPHA:264694
- Secondary interstitial lung disease specific to childhood associated with a systemic disease ORPHA:264699
- Secondary interstitial lung disease specific to childhood associated with a connective tissue disease ORPHA:264704
- 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
- Pediatric systemic lupus erythematosus ORPHA:93552
- Juvenile polymyositis ORPHA:93568
- Juvenile dermatomyositis ORPHA:93672
- Secondary interstitial lung disease specific to childhood associated with a systemic vasculitis ORPHA:264709
- Secondary interstitial lung disease specific to childhood associated with a granulomatous disease ORPHA:264714
- Secondary interstitial lung disease specific to childhood associated with a metabolic disease ORPHA:264719
- Familial hypocalciuric hypercalcemia ORPHA:405
- Familial hypocalciuric hypercalcemia type 1 ORPHA:93372
- Familial hypocalciuric hypercalcemia type 2 ORPHA:101049
- Familial hypocalciuric hypercalcemia type 3 ORPHA:101050
- Gaucher disease type 2 ORPHA:77260
- Gaucher disease type 3 ORPHA:77261
- Hermansky-Pudlak syndrome due to BLOC-3 deficiency ORPHA:231500
- Acid sphingomyelinase deficiency ORPHA:618899
- Autoimmune interstitial lung disease-arthritis syndrome ORPHA:444092
- SAMD9L-associated autoinflammatory syndrome ORPHA:619367
- Interstitial lung disease specific to adulthood ORPHA:264735
- Primary interstitial lung disease specific to adulthood ORPHA:264740
- Birt-Hogg-Dubé syndrome ORPHA:122
- Lymphangioleiomyomatosis ORPHA:538
- Autoimmune pulmonary alveolar proteinosis ORPHA:747
- Adult acute respiratory distress syndrome ORPHA:70578
- Idiopathic interstitial pneumonia ORPHA:98300
- Idiopathic pulmonary fibrosis ORPHA:2032
- Cryptogenic organizing pneumonia ORPHA:1302
- Acute interstitial pneumonia ORPHA:79126
- Respiratory bronchiolitis-interstitial lung disease syndrome ORPHA:79127
- Lymphoid interstitial pneumonia ORPHA:79128
- Non-specific interstitial pneumonia ORPHA:91364
- Desquamative interstitial pneumonia ORPHA:98852
- Combined pulmonary fibrosis-emphysema syndrome ORPHA:300564
- Idiopathic pleuroparenchymal fibroelastosis ORPHA:494428
- Pneumoconiosis ORPHA:182098
- Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome ORPHA:210136
- Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome ORPHA:221043
- Secondary interstitial lung disease specific to adulthood associated with a systemic disease ORPHA:264745
- Interstitial lung disease in childhood and adulthood ORPHA:264757
- Primary interstitial lung disease in childhood and adulthood ORPHA:264762
- Idiopathic pulmonary hemosiderosis ORPHA:99931
- Primary interstitial lung disease in childhood and adulthood due to alveolar structure disorder ORPHA:264930
- Chronic respiratory distress with surfactant metabolism deficiency ORPHA:217566
- Interstitial lung disease due to SP-C deficiency ORPHA:440392
- Primary interstitial lung disease in childhood and adulthood due to alveolar vascular disorder ORPHA:264935
- Secondary interstitial lung disease in childhood and adulthood ORPHA:264944
- Secondary pulmonary hemosiderosis ORPHA:99930
- Secondary interstitial lung disease in childhood and adulthood associated with a systemic disease ORPHA:264949
- Anti-glomerular basement membrane disease ORPHA:375
- Secondary interstitial lung disease in childhood and adulthood associated with a connective tissue disease ORPHA:182104
- Secondary interstitial lung disease in childhood and adulthood associated with a metabolic disease ORPHA:264968
- Niemann-Pick disease type C ORPHA:646
- Niemann-Pick disease type C, severe perinatal form ORPHA:216972
- Niemann-Pick disease type C, severe early infantile neurologic onset ORPHA:216975
- Niemann-Pick disease type C, late infantile neurologic onset ORPHA:216978
- Niemann-Pick disease type C, juvenile neurologic onset ORPHA:216981
- Niemann-Pick disease type C, adult neurologic onset ORPHA:216986
- Gaucher disease type 1 ORPHA:77259
- Secondary interstitial lung disease in childhood and adulthood associated with a systemic vasculitis ORPHA:264973
- Exposure-related interstitial lung disease ORPHA:264984
- Hypersensitivity pneumonitis ORPHA:31740
- Non-fibrotic hypersensitivity pneumonitis ORPHA:686462
- Fibrotic hypersensitivity pneumonitis ORPHA:686465
- Drug or radiation exposure-related interstitial lung disease ORPHA:264978
- Secondary pulmonary alveolar proteinosis ORPHA:420259
- Heiner syndrome ORPHA:99932
- Syndromic multisystem autoimmune disease due to Itch deficiency ORPHA:228426
- Primary ciliary dyskinesia-retinitis pigmentosa syndrome ORPHA:247522
- Pulmonary non-tuberculous mycobacterial infection ORPHA:411703
- Plastic bronchitis ORPHA:439881
- STING-associated vasculopathy with onset in infancy ORPHA:425120
- High altitude pulmonary edema ORPHA:330012
- Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome ORPHA:293987
- Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders ORPHA:505248
- Pneumonia caused by Pseudomonas aeruginosa infection ORPHA:90066
- Middle East respiratory syndrome ORPHA:576074
- Pleural empyema ORPHA:449266
- Avian influenza ORPHA:454836
- Ventilator-induced diaphragmatic dysfunction ORPHA:505395
- Haddad syndrome ORPHA:99803
- Congenital central hypoventilation syndrome ORPHA:661
- Pulmonary fungal infections in patients deemed at risk ORPHA:217080
- Apnea of prematurity ORPHA:99981
- RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome ORPHA:692812
- Pediatric acute respiratory distress syndrome ORPHA:685082
- Primary pulmonary tuberculosis ORPHA:645814
- Primary Sjögren syndrome ORPHA:289390
- Transient hyperammonemia of the newborn ORPHA:289877