Interstitial pulmonary disease

Symptom Information:

Symptom ID: HPO:0006530
Synonyms:
Interstitial lung disease [HPO:0006530]
Interstitial lung disease [Orphanet:33800]
Interstitial lung disease (disorder) [Orphanet:33800]
Fibrosis of lung (disorder) [Orphanet:33800]
Lung Diseases, Interstitial [Orphanet:33800]
Pulmonary Fibrosis [Orphanet:33800]
Interstitial lung disease [OMIM:Interstitial lung disease]
Interstitial pulmonary disease [OMIM:Interstitial pulmonary disease]
Interstitial/restrictive pneumopathy/restrictive respiratory syndrome [Orphanet:33800]
Pulmonary fibrosis [Orphanet:33800]
Pulmonary fibrosis [MedDRA:10037383]
Fibrosis lung [MedDRA:10037383]
Fibrosis pulmonary [MedDRA:10037383]
Lung fibrosis [MedDRA:10037383]
Other pulmonary fibroses NOS [MedDRA:10037383]
Postinflammatory pulmonary fibrosis [MedDRA:10037383]
Pulmonary fibrosis (post inflammatory) [MedDRA:10037383]
Pulmonary sclerosis [MedDRA:10037383]
Post inflammatory pulmonary fibrosis [MedDRA:10037383]
Lung scarring [MedDRA:10037383]
Interstitial lung disease [MedDRA:10022611]
Interstitial lung fibrosis [MedDRA:10022611]
Interstitial pneumonia [MedDRA:10022611]
Interstitial pneumonitis [MedDRA:10022611]
Interstitial pulmonary fibrosis [MedDRA:10022611]
Lung fibrosis interstitial [MedDRA:10022611]
Pneumonia interstitial [MedDRA:10022611]
Pneumonia interstitial diffuse [MedDRA:10022611]
Lymphoid interstitial pneumonia [MedDRA:10022611]
Acute diffuse infiltrative lung disease [MedDRA:10022611]
Respiratory bronchiolitis-associated interstitial lung disease [MedDRA:10022611]
RB-ILD [MedDRA:10022611]
Chronic interstitial pneumonia [MedDRA:10022611]
Interstitial pneumonia aggravated [MedDRA:10022611]
Follicular bronchiolitis [MedDRA:10022611]
Interstitial lung disease (rare) [OMIM:Interstitial lung disease (rare)]
Interstitial pneumonia [OMIM:Interstitial pneumonia]
Interstitial pulmonary fibrosis [OMIM:Interstitial pulmonary fibrosis]
Lung fibrosis [OMIM:Lung fibrosis]
Pulmonary fibrosis (classic feature) [OMIM:Pulmonary fibrosis (classic feature)]
Pneumonia, usual interstitial [OMIM,cm]
Quality:
Cross references:
Orphanet:33800 "Interstitial/restrictive pneumopathy/restrictive respiratory syndrome" [Orphanet:33800]
OMIM: "Interstitial lung disease" [OMIM:Interstitial lung disease]
OMIM: "Interstitial pulmonary disease" [OMIM:Interstitial pulmonary disease]
OMIM: "Interstitial lung disease (rare)" [OMIM:Interstitial lung disease (rare)]
OMIM: "Interstitial pneumonia" [OMIM:Interstitial pneumonia]
OMIM: "Interstitial pulmonary fibrosis" [OMIM:Interstitial pulmonary fibrosis]
OMIM: "Lung fibrosis" [OMIM:Lung fibrosis]
OMIM: "Pulmonary fibrosis (classic feature)" [OMIM:Pulmonary fibrosis (classic feature)]
UMLS:C0206062 "Lung Diseases, Interstitial" [Orphanet:33800]
UMLS:C0034069 "Pulmonary Fibrosis" [Orphanet:33800]
Is a (Direct Parents):
Orphanet Abnormality of the respiratory system
MedDRA Parenchymal lung disorders NEC
HPO         Abnormality of lung morphology
Orphanet Restrictive ventilatory defect
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of lung morphology(HPO:0002088)
                Interstitial pulmonary disease(HPO:0006530)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Lower respiratory tract disorders (excl obstruction and infection)(MedDRA:10024967)
       Parenchymal lung disorders NEC(MedDRA:10033979)
          Interstitial pulmonary disease(HPO:0006530)
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

AARSKOG SYNDROME, AUTOSOMAL DOMINANT (OMIM:100050)
Aarskog-Scott syndrome (Orphanet:915)
Acute interstitial pneumonia (Orphanet:79126)
Combined pulmonary fibrosis-emphysema syndrome (Orphanet:300564)
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome (Orphanet:306504)
Cryptogenic organizing pneumonia (Orphanet:1302)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 (OMIM:224230)
Desquamative interstitial pneumonia (Orphanet:98852)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
HERMANSKY-PUDLAK SYNDROME 1 (OMIM:203300)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY (OMIM:614700)
INFANTILE LIVER FAILURE SYNDROME 2 (OMIM:615486)
Idiopathic pulmonary fibrosis (Orphanet:2032)
Immunodeficiency with natural-killer cell deficiency (Orphanet:75391)
Lymphangioleiomyomatosis (Orphanet:538)
Lymphoid interstitial pneumonia (Orphanet:79128)
Neonatal acute respiratory distress with surfactant metabolism deficiency (Orphanet:217563)
Non-specific interstitial pneumonia (Orphanet:91364)
Respiratory bronchiolitis - interstitial lung disease (Orphanet:79127)
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET (OMIM:615934)
Sarcoidosis (Orphanet:797)
Sterile multifocal osteomyelitis with periostitis and pustulosis (Orphanet:210115)
Systemic sclerosis (Orphanet:90291)