List of rare lung diseases: Difference between revisions
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Latest revision as of 23:36, 12 July 2024
List of Rare Lung Diseases[edit]
- Acropectorovertebral dysplasia F form
- Acute interstitial pneumonia
- Allergic bronchopulmonary aspergillosis
- Alpha-1 antitrypsin deficiency
- Alveolar capillary dysplasia
- Arterial tortuosity syndrome
- Asbestosis
- Autoimmune pulmonary alveolar proteinosis
- Beryllium disease
- Birt-Hogg-Dube syndrome
- Blau syndrome
- Brain-lung-thyroid syndrome
- Bronchiolitis obliterans
- Bronchiolitis obliterans organizing pneumonia
- Bronchogenic cyst
- Bronchopulmonary dysplasia
- Cantu syndrome
- Catamenial pneumothorax
- Children's interstitial lung disease
- Chronic granulomatous disease
- Chronic thromboembolic pulmonary hypertension
- Classical-like Ehlers-Danlos syndrome
- Coal worker's pneumoconiosis
- Congenital diaphragmatic hernia
- Congenital lobar emphysema
- Congenital pulmonary alveolar proteinosis
- Congenital pulmonary lymphangiectasia
- Congenital tracheomalacia
- Cornelia de Lange syndrome
- Costocoracoid ligament congenitally short
- Cranioectodermal dysplasia
- CREST syndrome
- Cryptogenic organizing pneumonia
- Cutis laxa, autosomal dominant
- Cutis laxa, autosomal recessive type 1
- Cystic fibrosis
- Cystic medial necrosis of aorta
- Diffuse cutaneous systemic sclerosis
- Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia
- Diffuse panbronchiolitis
- Donnai-Barrow syndrome
- Eisenmenger syndrome
- Ellis-Van Creveld syndrome
- Emanuel syndrome
- Enthesitis-related juvenile idiopathic arthritis
- Eosinophilic granulomatosis with polyangiitis
- Familial hypocalciuric hypercalcemia type 1
- Familial hypocalciuric hypercalcemia type 2
- Familial hypocalciuric hypercalcemia type 3
- Familial mixed cryoglobulinemia
- Familial thoracic aortic aneurysm and dissection
- Familial thyroglossal duct cyst
- Feingold syndrome
- Fetal akinesia deformation sequence
- Fibrosing mediastinitis
- Froster-Huch syndrome
- Game Friedman Paradice syndrome
- Gaucher disease type 1
- Gaucher disease type 2
- Gaucher disease type 3
- Geroderma osteodysplastica
- Goodpasture syndrome
- Granulomatosis with polyangiitis
- Hashimoto-Pritzker syndrome
- Hemangiomatosis, familial pulmonary capillary
- Henoch-Schonlein purpura
- Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis
- Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
- Idiopathic acute eosinophilic pneumonia
- Idiopathic pulmonary fibrosis
- Idiopathic pulmonary hemosiderosis
- Intrahepatic cholestasis of pregnancy
- Jeune syndrome
- Juvenile dermatomyositis
- Juvenile polymyositis
- Kabuki syndrome
- Kaolin pneumoconiosis
- Kartagener syndrome
- Laryngoonychocutaneous syndrome - See Epidermolysis bullosa
- Lethal congenital contracture syndrome 1
- Limited cutaneous systemic sclerosis
- Limited systemic sclerosis
- Loeys-Dietz syndrome
- Loeys-Dietz syndrome type 1
- Loeys-Dietz syndrome type 2
- Loeys-Dietz syndrome type 3
- Loeys-Dietz syndrome type 4
- Lung agenesis
- Lymphangioleiomyomatosis
- Manouvrier syndrome
- Meconium aspiration syndrome
- Microphthalmia syndromic 9
- Microscopic polyangiitis
- Mixed connective tissue disease
- Mounier-Kuhn syndrome
- Multifocal fibrosclerosis
- Multisystemic smooth muscle dysfunction syndrome
- Niemann-Pick disease type B
- Nocardiosis
- Nontuberculous mycobacterial lung disease
- Occipital horn syndrome
- Orofaciodigital syndrome 4
- PAGOD syndrome
- Pallister-Killian mosaic syndrome
- Pentalogy of Cantrell
- Peroxisomal biogenesis disorders
- Pleuroparenchymal fibroelastosis
- Primary ciliary dyskinesia
- Psoriatic juvenile idiopathic arthritis
- Pulmonary alveolar microlithiasis
- Pulmonary sequestration
- Pulmonary venoocclusive disease
- Recurrent respiratory papillomatosis
- Respiratory distress syndrome, infant
- Sarcoidosis - Not a rare disease.
- SCARF syndrome
- Short rib-polydactyly syndrome type 3
- Short rib-polydactyly syndrome type 1
- Short rib-polydactyly syndrome type 4
- Short rib-polydactyly syndrome, Majewski type
- Silicosis
- Simpson-Golabi-Behmel syndrome
- Sprengel deformity
- Sudden infant death with dysgenesis of the testes syndrome
- Systemic onset juvenile idiopathic arthritis
- Thoracic dysplasia hydrocephalus syndrome
- Thoracolaryngopelvic dysplasia
- Thoracomelic dysplasia
- Tracheal agenesis
- Tracheobronchomalacia
- Tracheobronchopathia osteoplastica
- Vascular Ehlers-Danlos syndrome
- Wilson-Mikity syndrome
- Wolf-Hirschhorn syndrome
- Wrinkly skin syndrome
- Yellow nail syndrome
- Young syndrome
NIH genetic and rare disease info[edit]
List of rare lung diseases is a rare disease.
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Rare diseases - List of rare lung diseases
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