{"orpha":264992,"name":"Genetic interstitial lung disease","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Genetic ILD"],"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-264992/","orphanet_url":"https://www.orpha.net/en/disease/detail/264992","names":{"fr":{"name":"Pneumopathie interstitielle génétique","synonyms":["ILD génétique"]},"de":{"name":"Interstitielle Lungenkrankheit, genetisch bedingte","synonyms":["ILD, genetisch bedingte"]},"es":{"name":"Enfermedad pulmonar intersticial genética","synonyms":["EPI genética","ILD genética"]},"it":{"name":"Pneumopatia interstiziale genetica","synonyms":["ILD genetica"]},"nl":{"name":"Genetische interstitiële longziekte","synonyms":["Genetische ILD"]},"pt":{"name":"Doença pulmonar intersticial genética"},"pl":{"name":"Śródmiąższowa choroba płuc uwarunkowana genetycznie","synonyms":["ILD uwarunkowana genetycznie"]},"cs":{"name":"Geneticky podmíněná intersticiální plicní nemoc","synonyms":["Geneticky podmíněná ILD"]},"uk":{"name":"Генетично обумовлене інтерстиціальне захворювання легень","synonyms":["Генетична ILD"]},"zh":{"name":"遗传性间质性肺病","synonyms":["遗传性ILD"]},"tr":{"name":"Genetik interstisyel akciğer hastalığı","synonyms":["GenetiK ILD"]}},"xrefs":[{"source":"UMLS","code":"C5679736","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97955,"name":"Rare respiratory disease"},"parents":[{"orpha":156610,"name":"Rare genetic respiratory disease","classifications":[156]}],"children":[{"orpha":352629,"name":"16q24.1 microdeletion syndrome","type":"Disease"},{"orpha":618899,"name":"Acid sphingomyelinase deficiency","type":"Clinical group"},{"orpha":444092,"name":"Autoimmune interstitial lung disease-arthritis syndrome","type":"Disease"},{"orpha":217566,"name":"Chronic respiratory distress with surfactant metabolism deficiency","type":"Disease"},{"orpha":210122,"name":"Congenital alveolar capillary dysplasia","type":"Disease"},{"orpha":2414,"name":"Congenital pulmonary lymphangiectasia","type":"Disease"},{"orpha":621758,"name":"Fibrosis-neurodegeneration-cerebral angiomatosis syndrome","type":"Disease"},{"orpha":221043,"name":"Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome","type":"Disease"},{"orpha":440392,"name":"Interstitial lung disease due to SP-C deficiency","type":"Disease"},{"orpha":306504,"name":"Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome","type":"Disease"},{"orpha":137631,"name":"Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome","type":"Disease"},{"orpha":100049,"name":"Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}