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233703007: Interstitial lung disease (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2004. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
350185018 Interstitial lung disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
350186017 ILD - Interstitial lung disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
621923011 Interstitial lung disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3037993016 Diffuse parenchymal lung disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1848821000195113 interstiziopatia polmonare it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
208511000172110 pneumopathie interstitielle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
485201000172116 maladie pulmonaire interstitielle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
418551000274119 Interstitielle Lungenerkrankung de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3417591001000110 Interstitielle Lungenkrankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

57 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Interstitial lung disease Is a Disorder of lower respiratory system (disorder) false Inferred relationship Some
Interstitial lung disease Finding site Lung structure false Inferred relationship Some
Interstitial lung disease Is a Disorder of lung (disorder) true Inferred relationship Some
Interstitial lung disease Is a Disorder of soft tissue of thoracic cavity true Inferred relationship Some
Interstitial lung disease Is a Disorder of soft tissue of trunk false Inferred relationship Some
Interstitial lung disease Is a Disorder of connective tissue (disorder) true Inferred relationship Some
Interstitial lung disease Finding site Structure of interstitial tissue of lung true Inferred relationship Some 1
Interstitial lung disease Is a Connective tissue disorder by body site false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Pulmonary hypostasis Is a True Interstitial lung disease Inferred relationship Some
Diffuse infiltrative lung disease Is a False Interstitial lung disease Inferred relationship Some
Respiratory bronchiolitis associated interstitial lung disease (disorder) Is a False Interstitial lung disease Inferred relationship Some
Pulmonary edema Is a False Interstitial lung disease Inferred relationship Some
Pulmonary eosinophilic granuloma Is a False Interstitial lung disease Inferred relationship Some
Fibrosis of lung Is a False Interstitial lung disease Inferred relationship Some
Drug-induced interstitial lung disorder (disorder) Is a True Interstitial lung disease Inferred relationship Some
Pulmonary congestion and hypostasis Is a True Interstitial lung disease Inferred relationship Some
Trauma and postoperative pulmonary insufficiency Is a False Interstitial lung disease Inferred relationship Some
Other alveolar and parietoalveolar disease Is a False Interstitial lung disease Inferred relationship Some
Interstitial lung disease NEC Is a False Interstitial lung disease Inferred relationship Some
[X]Other respiratory diseases principally affecting the interstitium Is a False Interstitial lung disease Inferred relationship Some
[X]Other interstitial pulmonary diseases with fibrosis Is a False Interstitial lung disease Inferred relationship Some
[X]Other specified interstitial pulmonary diseases Is a False Interstitial lung disease Inferred relationship Some
GIP - Giant cell interstitial pneumonitis Is a False Interstitial lung disease Inferred relationship Some
Interstitial pneumonia Is a False Interstitial lung disease Inferred relationship Some
Acute respiratory distress syndrome (disorder) Is a True Interstitial lung disease Inferred relationship Some
Interstitial emphysema of lung Is a True Interstitial lung disease Inferred relationship Some
infection au VIH causant une pneumopathie lymphoïde interstitielle Is a False Interstitial lung disease Inferred relationship Some
[X]Hepatopulmonary syndrome Is a False Interstitial lung disease Inferred relationship Some
Seasonal cryptogenic organizing pneumonia with biochemical cholestasis Is a False Interstitial lung disease Inferred relationship Some
Lymphoid interstitial pneumonitis Is a False Interstitial lung disease Inferred relationship Some
Idiopathic fibrosing alveolitis NOS Is a False Interstitial lung disease Inferred relationship Some
pneumonie non infectieuse Is a False Interstitial lung disease Inferred relationship Some
Pneumonia due to parasitic infestation Is a False Interstitial lung disease Inferred relationship Some
Postoperative pneumonia Is a False Interstitial lung disease Inferred relationship Some
Bacterial pneumonia Is a False Interstitial lung disease Inferred relationship Some
Pleurobronchopneumonia Is a False Interstitial lung disease Inferred relationship Some
Parainfluenza virus pneumonia Is a False Interstitial lung disease Inferred relationship Some
Pneumonia caused by respiratory syncytial virus (disorder) Is a False Interstitial lung disease Inferred relationship Some
Interstitial lung disease due to collagen vascular disease (disorder) Is a True Interstitial lung disease Inferred relationship Some
Rickettsial pneumonia Is a False Interstitial lung disease Inferred relationship Some
Pneumonia caused by pleuropneumonia-like organism Is a False Interstitial lung disease Inferred relationship Some
Pittsburgh pneumonia Is a False Interstitial lung disease Inferred relationship Some
Rheumatic pneumonitis Is a False Interstitial lung disease Inferred relationship Some
Parainfluenza virus bronchopneumonia Is a False Interstitial lung disease Inferred relationship Some
Surfactant dysfunction Is a False Interstitial lung disease Inferred relationship Some
Pulmonary interstitial glycogenosis Is a True Interstitial lung disease Inferred relationship Some
Chronic pneumonitis of infancy (disorder) Is a False Interstitial lung disease Inferred relationship Some
Neuroendocrine cell hyperplasia of infancy (disorder) Is a True Interstitial lung disease Inferred relationship Some
Diffuse interstitial rheumatoid disease of lung Is a True Interstitial lung disease Inferred relationship Some
Interstitial lung disease of childhood Is a True Interstitial lung disease Inferred relationship Some
Interstitial lung disease due to connective tissue disease Is a True Interstitial lung disease Inferred relationship Some
Malarial shock lung Is a True Interstitial lung disease Inferred relationship Some
Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome Is a True Interstitial lung disease Inferred relationship Some
Interstitial lung disease due to systemic disease Is a True Interstitial lung disease Inferred relationship Some
Interstitial lung disease due to granulomatous disease (disorder) Is a True Interstitial lung disease Inferred relationship Some
Interstitial lung disease due to metabolic disease (disorder) Is a True Interstitial lung disease Inferred relationship Some
Interstitial lung disease co-occurrent and due to systemic vasculitis (disorder) Is a False Interstitial lung disease Inferred relationship Some
A partial autosomal monosomy characterized clinically by lethal pulmonary disease that presents as severe respiratory distress and refractory pulmonary hypertension within a few hours after birth and typically results in death from respiratory failure within the first months of life. Characteristic histological features of lung tissue include paucity of alveolar wall capillaries, alveolar wall thickening, muscular hypertrophy of the pulmonary arteries, and malposition of the small pulmonary veins. Various additional congenital malformations may be associated, mostly gastrointestinal (intestinal malrotation and atresias, anular pancreas), genitourinary (dilatation of urinary tracts, duplicated uterus) and cardiovascular anomalies (hypoplastic left heart and other congenital heart defects). Is a True Interstitial lung disease Inferred relationship Some
Genetic disorder of surfactant dysfunction Is a True Interstitial lung disease Inferred relationship Some
Idiopathic pulmonary hemosiderosis Is a True Interstitial lung disease Inferred relationship Some
Pulmonary lymphangioleiomyomatosis Is a True Interstitial lung disease Inferred relationship Some
Diffuse pulmonary calcinosis Is a True Interstitial lung disease Inferred relationship Some
Diffuse pulmonary neurofibromatosis Is a True Interstitial lung disease Inferred relationship Some
Perinatal interstitial emphysema Is a True Interstitial lung disease Inferred relationship Some
Fetal interstitial neoplasm of lung Is a True Interstitial lung disease Inferred relationship Some
Interstitial lung disease due to juvenile polymyositis Is a True Interstitial lung disease Inferred relationship Some
Interstitial pulmonary fibrosis due to inhalation of substance Is a True Interstitial lung disease Inferred relationship Some
A rare genetic interstitial lung disease characterized by diffuse lung disease of variable phenotype ranging from severe respiratory insufficiency in infancy to asymptomatic adults, due to surfactant protein C deficiency. Typical presentation in infancy includes dyspnea, cough, wheezing, and gradual cyanosis, with or without failure to thrive. Radiological findings include diffuse ground-glass opacities in neonates, later interstitial thickening associated with lung hyperinflation, intraparenchymal/subpleural cysts, honeycombing, subpleural nodules, or bronchiectasis. Infiltrates and air leaks are frequent complications. Is a True Interstitial lung disease Inferred relationship Some
A rare genetic respiratory disease characterized by a variable clinical outcome ranging from a fatal respiratory distress syndrome in the neonatal period to chronic interstitial lung disease developing in infancy or childhood with chronic cough, rapid breathing, shortness of breath and recurrent pulmonary infections. Clinical manifestations of respiratory failure include grunting, intercostal retractions, nasal flaring, cyanosis, and progressive dyspnea. Is a True Interstitial lung disease Inferred relationship Some
A rare genetic systemic or rheumatologic disease characterized by interstitial lung disease (often with pulmonary hemorrhage) and inflammatory arthritis, associated with high-titer autoantibodies (including anti-nuclear and anti-neutrophil cytoplasmic antibodies, and rheumatoid factor). Patients present from infancy to adolescence with tachypnea, cough, hemoptysis, and/or joint pain. Some patients may also develop glomerular disease. Is a True Interstitial lung disease Inferred relationship Some
A rare, genetic interstitial lung disease characterised by accumulation of lipoproteins in the pulmonary alveoli leading to restrictive lung disease and respiratory failure. Patients present with dyspnoea, tachypnoea, cough, failure to thrive, and digital clubbing. Liver disease have been described in some cases including hepatomegaly, steatosis, fibrosis or cirrhosis. Is a True Interstitial lung disease Inferred relationship Some
Diffuse pulmonary meningotheliomatosis (disorder) Is a True Interstitial lung disease Inferred relationship Some
Interstitial lung disease due to vaping (disorder) Is a True Interstitial lung disease Inferred relationship Some
Interstitial lung disorder due to dabbing Is a True Interstitial lung disease Inferred relationship Some
Pulmonary hypertension due to interstitial lung disease (disorder) Due to True Interstitial lung disease Inferred relationship Some 2
Interstitial lung disease due to and following radiotherapy (disorder) Is a True Interstitial lung disease Inferred relationship Some
A rare idiopathic interstitial pneumonia characterized by prominent subpleural and parenchymal fibroelastosis and pleural fibrosis, predominantly involving the upper lobes. Signs and symptoms include non-productive cough, dyspnea, and recurrent respiratory infections. Pneumothorax is a frequently reported complication. Pulmonary function test reveals a restrictive pattern and reduced diffusing capacity. Computed tomography shows pleural thickening with signs of fibrosis (traction bronchiectasis, architectural distortion, and loss of volume), and reticulation. Is a True Interstitial lung disease Inferred relationship Some
Acute exacerbation of idiopathic pulmonary fibrosis (disorder) Is a True Interstitial lung disease Inferred relationship Some
A rare disease, manifesting with idiopathic pulmonary fibrosis, hepatic nodular regenerative hyperplasia leading to portal hypertension and thrombocytopenia due to bone marrow hypoplasia. The condition was associated with 100% mortality. Is a True Interstitial lung disease Inferred relationship Some
Familial idiopathic pulmonary fibrosis (disorder) Is a True Interstitial lung disease Inferred relationship Some
A rare interstitial lung disease characterized by early-onset, severe, progressive lung disease manifesting by respiratory distress, neurological symptoms including axial hypotonia, developmental delay, irritability, dystonia, poor visual contact and seizures, and variable multisystemic involvement including malabsorption, progressive growth failure, recurrent infections, chronic hemolytic anemia and liver dysfunction. Kidney dysfunction, cardiac involvement including cardiomegaly and cardiac hypertrophy, decreased vision and strabismus have also been reported. Lung fibrosis may cause death in infancy from respiratory failure. Is a True Interstitial lung disease Inferred relationship Some
Lung disease, immunodeficiency, chromosome breakage syndrome (disorder) Is a True Interstitial lung disease Inferred relationship Some

This concept is not in any reference sets

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