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113254000: Structure of interstitial tissue of lung (body structure)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
187041014 Interstitial tissue of lung en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
382405010 Structure of interstitial tissue of lung en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
647925016 Structure of interstitial tissue of lung (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
277621000077118 structure du tissu interstitiel du poumon fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Structure of interstitial tissue of lung Is a Lung part true Inferred relationship Some
Structure of interstitial tissue of lung Is a Structure of soft tissue of thorax (body structure) false Inferred relationship Some
Structure of interstitial tissue of lung Is a Interstitial tissue true Inferred relationship Some
Structure of interstitial tissue of lung partie de Entire lung false Additional relationship Some
Structure of interstitial tissue of lung Is a Connective tissue by site false Inferred relationship Some
Structure of interstitial tissue of lung Is a Structure of connective tissue of thorax (body structure) true Inferred relationship Some
Structure of interstitial tissue of lung Laterality Side (qualifier value) true Inferred relationship Some
Structure of interstitial tissue of lung Is a Structure of soft tissue of thoracic cavity (body structure) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Pneumonia due to parasitic infestation Finding site False Structure of interstitial tissue of lung Inferred relationship Some 2
Capillaria aerophila chest infection (disorder) Finding site False Structure of interstitial tissue of lung Inferred relationship Some 4
Pneumonia caused by Ascaris Finding site False Structure of interstitial tissue of lung Inferred relationship Some 2
Cryptogenic organizing pneumonia (disorder) Finding site False Structure of interstitial tissue of lung Inferred relationship Some 6
Malarial shock lung Finding site False Structure of interstitial tissue of lung Inferred relationship Some 3
Malarial shock lung Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome Finding site True Structure of interstitial tissue of lung Inferred relationship Some 2
Interstitial lung disease due to systemic disease Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Interstitial lung disease due to granulomatous disease (disorder) Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Interstitial lung disease due to metabolic disease (disorder) Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Interstitial lung disease co-occurrent and due to systemic vasculitis (disorder) Finding site True Structure of interstitial tissue of lung Inferred relationship Some 2
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). Finding site True Structure of interstitial tissue of lung Inferred relationship Some 3
Acute respiratory distress in newborn with surfactant disorder Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Genetic disorder of surfactant dysfunction Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Chronic respiratory distress with surfactant metabolism deficiency is a rare, genetic, primary interstitial lung disease with a highly variable clinical presentation, ranging from neonatal respiratory distress syndrome to mild to severe interstitial lung disease (typical symptoms include cough, tachypnea, hypoxia, clubbing, crackles, failure to thrive). Lung biopsy reveals diffuse alveolar damage, interstitial thickening with inflammatory infiltrates, fibroblast proliferation, collagen deposition, and multiple foci of fibrosis, alveolar type II cell hyperplasia, abundant foamy alveolar macrophages and granular lipoproteic material in the alveolar lumen. Imaging shows cystic spaces and ground-glass opacities that are typically homogenously diffuse. Finding site True Structure of interstitial tissue of lung Inferred relationship Some 2
Acute exacerbation of idiopathic pulmonary fibrosis (disorder) Finding site True Structure of interstitial tissue of lung Inferred relationship Some 2
Idiopathic pulmonary hemosiderosis Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Perinatal interstitial emphysema Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Acute respiratory distress syndrome due to disease caused by severe acute respiratory syndrome coronavirus 2 (disorder) Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Fetal interstitial neoplasm of lung Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Interstitial lung disease due to juvenile polymyositis Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Interstitial pneumonitis with autoimmune features Finding site False Structure of interstitial tissue of lung Inferred relationship Some 1
Interstitial pulmonary fibrosis due to inhalation of substance Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Interstitial pulmonary fibrosis due to inhalation of drug Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
fibrose pulmonaire chronique causée par des vapeurs chimiques Finding site False Structure of interstitial tissue of lung Inferred relationship Some 1
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. Finding site True Structure of interstitial tissue of lung Inferred relationship Some 2
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. Finding site True Structure of interstitial tissue of lung Inferred relationship Some 2
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. Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
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. Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
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. Finding site True Structure of interstitial tissue of lung Inferred relationship Some 2
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. Finding site True Structure of interstitial tissue of lung Inferred relationship Some 3
Diffuse pulmonary meningotheliomatosis (disorder) Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Interstitial lung disease due to vaping (disorder) Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Interstitial lung disorder due to dabbing Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Acute respiratory distress syndrome due to dabbing Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Acute respiratory distress syndrome due to vaping (disorder) Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Interstitial lung disease due to and following radiotherapy (disorder) Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
Chronic pulmonary fibrosis caused by vapor (disorder) Finding site True Structure of interstitial tissue of lung Inferred relationship Some 1
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. Finding site True Structure of interstitial tissue of lung Inferred relationship Some 2
Lung disease, immunodeficiency, chromosome breakage syndrome (disorder) Finding site True Structure of interstitial tissue of lung Inferred relationship Some 2

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Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

Anatomy structure and entire association reference set (foundation metadata concept)

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