Lung Diseases | Page 1

135 diseases found in 2 pages

A 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

B Diseases

Beryllium disease Birt-Hogg-Dube syndrome Blau syndrome Brain-lung-thyroid syndrome Bronchiolitis obliterans Bronchiolitis obliterans organizing pneumonia Bronchogenic cyst Bronchopulmonary dysplasia

C Diseases

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

D Diseases

Diffuse cutaneous systemic sclerosis Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia Diffuse panbronchiolitis Donnai-Barrow syndrome

E Diseases

Eisenmenger syndrome Ellis-Van Creveld syndrome Emanuel syndrome Enthesitis-related juvenile idiopathic arthritis Eosinophilic granulomatosis with polyangiitis

F Diseases

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

G Diseases

Game Friedman Paradice syndrome Gaucher disease type 1 Gaucher disease type 2 Gaucher disease type 3 Geroderma osteodysplastica Goodpasture syndrome Granulomatosis with polyangiitis

H Diseases

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

I Diseases

Idiopathic acute eosinophilic pneumonia Idiopathic pulmonary fibrosis Idiopathic pulmonary hemosiderosis Intrahepatic cholestasis of pregnancy

J Diseases

Jeune syndrome Juvenile dermatomyositis Juvenile polymyositis

K Diseases

Kabuki syndrome Kaolin pneumoconiosis Kartagener syndrome

L Diseases

Laryngoonychocutaneous syndrome 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

M Diseases

Manouvrier syndrome Meconium aspiration syndrome Microphthalmia syndromic 9 Microscopic polyangiitis Mixed connective tissue disease Mounier-Kuhn syndrome Multifocal fibrosclerosis Multisystemic smooth muscle dysfunction syndrome

N Diseases

Niemann-Pick disease type B Nocardiosis Nontuberculous mycobacterial lung disease

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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