{"orpha":101944,"name":"Rare pulmonary disease","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-101944/","orphanet_url":"https://www.orpha.net/en/disease/detail/101944","names":{"fr":{"name":"Maladie pulmonaire rare"},"de":{"name":"Lungenkrankheit, seltene"},"es":{"name":"Enfermedad pulmonar rara"},"it":{"name":"Malattia polmonare rara"},"nl":{"name":"Zeldzame longziekte"},"pt":{"name":"Doença pulmonar, rara"},"pl":{"name":"Rzadkie choroby płuc"},"cs":{"name":"Vzácné plicní onemocnění"},"uk":{"name":"Рідкісне легеневе захворювання"},"zh":{"name":"罕见肺部疾病"},"tr":{"name":"Nadir akciğer hastalığı"}},"xrefs":[{"source":"MONDO","code":"15118","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681796","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":2112,"name":"OBSOLETE: Follicular hamartoma-alopecia-cystic fibrosis syndrome","status":"inactive"}],"preferential_parent":{"orpha":97955,"name":"Rare respiratory disease"},"parents":[{"orpha":97955,"name":"Rare respiratory disease","classifications":[184]}],"children":[{"orpha":178320,"name":"Acute lung injury","type":"Particular clinical situation in a disease or syndrome"},{"orpha":1164,"name":"Allergic bronchopulmonary aspergillosis","type":"Disease"},{"orpha":60,"name":"Alpha-1-antitrypsin deficiency","type":"Disease"},{"orpha":99981,"name":"Apnea of prematurity","type":"Disease"},{"orpha":454836,"name":"Avian influenza","type":"Disease"},{"orpha":1303,"name":"Bronchiolitis obliterans","type":"Clinical group"},{"orpha":661,"name":"Congenital central hypoventilation syndrome","type":"Disease"},{"orpha":2140,"name":"Congenital diaphragmatic hernia","type":"Morphological anomaly"},{"orpha":586,"name":"Cystic fibrosis","type":"Disease"},{"orpha":90060,"name":"Diffuse alveolar hemorrhage","type":"Clinical syndrome"},{"orpha":171700,"name":"Diffuse panbronchiolitis","type":"Disease"},{"orpha":2903,"name":"Familial spontaneous pneumothorax","type":"Disease"},{"orpha":99803,"name":"Haddad syndrome","type":"Malformation syndrome"},{"orpha":330012,"name":"High altitude pulmonary edema","type":"Particular clinical situation in a disease or syndrome"},{"orpha":60033,"name":"Idiopathic bronchiectasis","type":"Disease"},{"orpha":70590,"name":"Infantile apnea","type":"Disease"},{"orpha":182095,"name":"Interstitial lung disease","type":"Category"},{"orpha":389,"name":"Langerhans cell histiocytosis","type":"Disease"},{"orpha":70588,"name":"Meconium aspiration syndrome","type":"Disease"},{"orpha":576074,"name":"Middle East respiratory syndrome","type":"Disease"},{"orpha":505248,"name":"Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders","type":"Malformation syndrome"},{"orpha":685082,"name":"Pediatric acute respiratory distress syndrome","type":"Disease"},{"orpha":439881,"name":"Plastic bronchitis","type":"Particular clinical situation in a disease or syndrome"},{"orpha":449266,"name":"Pleural empyema","type":"Particular clinical situation in a disease or syndrome"},{"orpha":90066,"name":"Pneumonia caused by Pseudomonas aeruginosa infection","type":"Particular clinical situation in a disease or syndrome"},{"orpha":289390,"name":"Primary Sjögren disease","type":"Disease"},{"orpha":244,"name":"Primary ciliary dyskinesia","type":"Disease"},{"orpha":247522,"name":"Primary ciliary dyskinesia-retinitis pigmentosa syndrome","type":"Disease"},{"orpha":645814,"name":"Primary pulmonary tuberculosis","type":"Clinical subtype"},{"orpha":2038,"name":"Pulmonary arteriovenous malformation","type":"Morphological anomaly"},{"orpha":217080,"name":"Pulmonary fungal infections in patients deemed at risk","type":"Particular clinical situation in a disease or syndrome"},{"orpha":60026,"name":"Pulmonary nodular lymphoid hyperplasia","type":"Disease"},{"orpha":411703,"name":"Pulmonary non-tuberculous mycobacterial infection","type":"Disease"},{"orpha":692812,"name":"RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome","type":"Disease"},{"orpha":293987,"name":"Rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome","type":"Disease"},{"orpha":60032,"name":"Recurrent respiratory papillomatosis","type":"Disease"},{"orpha":425120,"name":"STING-associated vasculopathy with onset in infancy","type":"Disease"},{"orpha":140896,"name":"Severe acute respiratory syndrome","type":"Disease"},{"orpha":3167,"name":"Siegler-Brewer-Carey syndrome","type":"Malformation syndrome"},{"orpha":36238,"name":"Staphylococcal necrotizing pneumonia","type":"Disease"},{"orpha":168593,"name":"Sudden infant death-dysgenesis of the testes syndrome","type":"Malformation syndrome"},{"orpha":228426,"name":"Syndromic multisystem autoimmune disease due to Itch deficiency","type":"Disease"},{"orpha":90291,"name":"Systemic sclerosis","type":"Disease"},{"orpha":3348,"name":"Tracheobronchopathia osteochondroplastica","type":"Disease"},{"orpha":505395,"name":"Ventilator-induced diaphragmatic dysfunction","type":"Particular clinical situation in a disease or syndrome"},{"orpha":3471,"name":"Young syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}