Lung diseases

• 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
• Cryoglobulinemic vasculitis
• 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 thoracic aortic aneurysm and aortic 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
• Tracheal agenesis
• Tracheobronchomalacia
• Tracheobronchopathia osteoplastica
• Vascular Ehlers-Danlos syndrome
• Wolf-Hirschhorn syndrome
• Wrinkly skin syndrome
• Yellow nail syndrome
• Young syndrome

NIH genetic and rare disease info

• NIH info on Lung diseases

Lung diseases is a rare disease.