Item
MDT board diagnosis available?
integer
Code List
MDT board diagnosis available?
Item
MDT diagnosis based on: Clinical data
integer
Code List
MDT diagnosis based on: Clinical data
Item
Radiological data
integer
Code List
Radiological data
Item
Pathological data
integer
Code List
Pathological data
Item
Interstitial Lung Abnormalities (ILA)
integer
Code List
Interstitial Lung Abnormalities (ILA)
Item
Idiopathic Interstitial Pneumonia (IIP)
integer
Code List
Idiopathic Interstitial Pneumonia (IIP)
Item
Idiopathic Pulmonary Fibrosis (IPF)
integer
Code List
Idiopathic Pulmonary Fibrosis (IPF)
Item
Likelihood of diagnosis
text
Code List
Likelihood of diagnosis
CL Item
Definite IPF diagnosis (definite)
CL Item
Provisional high-confidence IPF diagnosis (highconf)
CL Item
Provisional low-confidence IPF diagnosis (lowconf)
Item
Non-Specific Interstitial Pneumonia (NSIP)
integer
Code List
Non-Specific Interstitial Pneumonia (NSIP)
CL Item
Cellular (cellular)
CL Item
Fibrotic (fibrotic)
Item
Respiratory-Bronchiolitis-ILD
integer
Code List
Respiratory-Bronchiolitis-ILD
Item
Desquamative Interstitial Pneumonia (DIP)
integer
Code List
Desquamative Interstitial Pneumonia (DIP)
Item
Cryptogenic Organizing Pneumonia (COP)
integer
Code List
Cryptogenic Organizing Pneumonia (COP)
Item
Acute Interstitial Pneumonia (AIP)
integer
Code List
Acute Interstitial Pneumonia (AIP)
Item
Lymphoid Interstitial Pneumonia (LIP)
integer
Code List
Lymphoid Interstitial Pneumonia (LIP)
Item
Idiopathic Pleuroparenchymal Fibroelastosis (PPFE)
integer
Code List
Idiopathic Pleuroparenchymal Fibroelastosis (PPFE)
Item
Bronchiolocentric form of IIP
integer
Code List
Bronchiolocentric form of IIP
Item
Acute Fibrinous and Organizing Pneumonia (AFOP)
integer
Code List
Acute Fibrinous and Organizing Pneumonia (AFOP)
Item
Unclassifiable IIP
integer
Code List
Unclassifiable IIP
Item
Meets IPAF criteria?
integer
Code List
Meets IPAF criteria?
Item
Granulomatous lung diseases of non-infectious origin
integer
Code List
Granulomatous lung diseases of non-infectious origin
Item
Type of granulomatous lung disease
text
Code List
Type of granulomatous lung disease
CL Item
Sarcoidosis (sarc)
CL Item
Granulomatosis with polyangiitis (GPA) (gpa)
CL Item
Bronchiolocentric granulomatosis (brongra)
CL Item
Aspiration pneumonia (asppneu)
CL Item
Hypersensitivity pneumonitis (hp)
Item
Sarcoidosis stage according to chest X-ray
text
Code List
Sarcoidosis stage according to chest X-ray
CL Item
0 - no visible lung or mediastinal involvement (0)
CL Item
I - bihilar lymphadenopathia w/o lung involvement (I)
CL Item
II - bihilar lymphadenopathia and lung involvement (II)
CL Item
III - lung involvement in absence of bihilar lymphadenopathia (III)
CL Item
IV - lung fibrosis (IV)
Item
Extrapulmonary organ manifestation of sarcoidosis null
integer
Code List
Extrapulmonary organ manifestation of sarcoidosis null
Item
Type of Hypersensitivity pneumonitis
text
Code List
Type of Hypersensitivity pneumonitis
CL Item
Fibrotic (fibrotic)
CL Item
Non-fibrotic (nonfib)
Item
ILD due to inhaled inorganic agents Please specify the causing agent in the section environmental exposure
integer
Code List
ILD due to inhaled inorganic agents Please specify the causing agent in the section environmental exposure
Item
Carbon compounds
integer
Code List
Carbon compounds
Item
ILD due to inhaled organic agents (non-allergic, no HP) - inhaled or aspired- Please specify the causing agent in the section environmental exposure
integer
Code List
ILD due to inhaled organic agents (non-allergic, no HP) - inhaled or aspired- Please specify the causing agent in the section environmental exposure
Item
ILD in the context of rheumatoid arthritis or collagen/vascular disease
integer
Code List
ILD in the context of rheumatoid arthritis or collagen/vascular disease
Item
Anti-synthetase syndrome (Jo-1-Syndrome)
integer
Code List
Anti-synthetase syndrome (Jo-1-Syndrome)
Item
Polymyositis/Dermatomyositis
integer
Code List
Polymyositis/Dermatomyositis
Item
Sjögren's Disease
integer
Code List
Sjögren's Disease
Item
Unclassifiable CVD-ILD
integer
Code List
Unclassifiable CVD-ILD
Item
ILD in the context of a dysbalanced immune system
integer
Code List
ILD in the context of a dysbalanced immune system
CL Item
Common variable immunodeficiency syndrome (CVID) - ILD (cvid)
CL Item
IgG4-related disease (igg4)
CL Item
ILD in the context of inflammatory bowel disease (infbowel)
CL Item
Crohn's disease (crohn)
CL Item
Ulcerative colitis (colitis)
Item
Eosinophilic ILDs
integer
Code List
Eosinophilic ILDs
CL Item
Acute eosinophilic pneumonia (AEP) (aep)
CL Item
Chronic eosinophilic pneumonia (CEP) (chroniceospneu)
CL Item
Eosinophilic granulomatosis with polyangiitis (EGPA) (agpa)
Item
ILD in the context of semi-malignant or malignant diseases
integer
Code List
ILD in the context of semi-malignant or malignant diseases
CL Item
Lymphangioleiomyomatosis (LAM) (lam)
CL Item
Pulmonary Langerhans Cell Histioystosis (LCH) (lch)
CL Item
Neurofibromatosis ILD (neurofibro)
CL Item
Birt-Hogg-Dubé-Syndrome (Cystic lung disease) (bhds)
Item
ILD in the context of a "storage" / "deposition" diseases
integer
Code List
ILD in the context of a "storage" / "deposition" diseases
CL Item
Hermansky-Pudlack syndrome (hpsip)
CL Item
Nieman Pick Disease (npd)
CL Item
Gauchers's Disease (gauchers)
CL Item
Pulmonary alveolar proteinosis (PAP) (pap)
CL Item
Amyloidosis (amyloidosis)
CL Item
Alveolar microlithiasis (Alveolarmicro)
Item
ILD due to medical measures Please specify in ILD-related drugs and medical measures
integer
Code List
ILD due to medical measures Please specify in ILD-related drugs and medical measures
CL Item
Post-ventilation ILD (postvent)
CL Item
Radiation induced ILD (radioild)
Item
ILD due to drugs (acc. to pneumotox) Please specify in ILD-related drugs and medical measures
integer
Code List
ILD due to drugs (acc. to pneumotox) Please specify in ILD-related drugs and medical measures
Item
Unclassifiable ILD
integer
Code List
Unclassifiable ILD
mdt_ild_rare
Item
Any rare ILD not listed above
text
Item
Familial form of ILD Please specify in Family history
integer
Code List
Familial form of ILD Please specify in Family history
CL Item
Familial IIP (familial)
CL Item
Hermansky-Pudlack Syndrom (hps)
CL Item
Telomeropathia (Telomeropathia)
CL Item
Alveolar microlithiasis (Alveolarmicro)
mdt_subfamilialother
Item
text
Item
CPFE criteria fulfilled
integer
Code List
CPFE criteria fulfilled