Pulmonary fibrosis

Symptom Information:

Symptom ID: HPO:0002206
Synonyms:
Lung fibrosis [Orphanet:32760]
Fibrosis of lung (disorder) [Orphanet:32760]
Pulmonary Fibrosis [Orphanet:32760]
Pulmonary fibrosis [OMIM:Pulmonary fibrosis]
Pulmonary fibrosis [Orphanet:32760]
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]
Lung fibrosis [OMIM:Lung fibrosis]
Pulmonary fibrosis (classic feature) [OMIM:Pulmonary fibrosis (classic feature)]
Quality:
Cross references:
Orphanet:32760 "Lung fibrosis" [Orphanet:32760]
OMIM: "Pulmonary fibrosis" [OMIM:Pulmonary fibrosis]
OMIM: "Lung fibrosis" [OMIM:Lung fibrosis]
OMIM: "Pulmonary fibrosis (classic feature)" [OMIM:Pulmonary fibrosis (classic feature)]
UMLS:C0034069 "Pulmonary Fibrosis" [Orphanet:32760]
Is a (Direct Parents):
MedDRA Parenchymal lung disorders NEC
Orphanet Abnormality of the diaphragm
HPO         Abnormality of lung morphology
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)
                Pulmonary fibrosis(HPO:0002206)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Lower respiratory tract disorders (excl obstruction and infection)(MedDRA:10024967)
       Parenchymal lung disorders NEC(MedDRA:10033979)
          Pulmonary fibrosis(HPO:0002206)
Database Frequency: 51 / 7739
Resource:

All diseases associated with this symptom:

46,XX gonadal dysgenesis (Orphanet:243)
Acute interstitial pneumonia (Orphanet:79126)
Alström syndrome (Orphanet:64)
Antisynthetase syndrome (Orphanet:81)
Braddock syndrome (Orphanet:52047)
Bronchiolitis obliterans with obstructive pulmonary disease (Orphanet:1303)
CREST syndrome (Orphanet:90290)
Combined pulmonary fibrosis-emphysema syndrome (Orphanet:300564)
Cryptogenic organizing pneumonia (Orphanet:1302)
Cystic fibrosis (Orphanet:586)
Cystic hamartoma of lung and kidney (Orphanet:2111)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 (OMIM:127550)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 (OMIM:613989)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 (OMIM:613990)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 (OMIM:224230)
Dermatomyositis (Orphanet:221)
Desquamative interstitial pneumonia (Orphanet:98852)
Diffuse cutaneous systemic sclerosis (Orphanet:220393)
Dyskeratosis congenita (Orphanet:1775)
Erdheim-Chester disease (Orphanet:35687)
Farber lipogranulomatosis (Orphanet:333)
Felty syndrome (Orphanet:47612)
Gaucher disease (Orphanet:355)
Gaucher disease type 3 (Orphanet:77261)
Granulomatosis with polyangiitis (Orphanet:900)
HERMANSKY-PUDLAK SYNDROME 4 (OMIM:614073)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hermansky-Pudlak syndrome with neutropenia (Orphanet:183678)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Idiopathic pulmonary fibrosis (Orphanet:2032)
Idiopathic pulmonary hemosiderosis (Orphanet:99931)
Immunodeficiency with natural-killer cell deficiency (Orphanet:75391)
Juvenile dermatomyositis (Orphanet:93672)
Limited cutaneous systemic sclerosis (Orphanet:220402)
Limited systemic sclerosis (Orphanet:220407)
Lung fibrosis - immunodeficiency - 46,XX gonadal dysgenesis (Orphanet:137631)
Lymphoid interstitial pneumonia (Orphanet:79128)
Mixed connective tissue disease (Orphanet:809)
Mulibrey nanism (Orphanet:2576)
Non-specific interstitial pneumonia (Orphanet:91364)
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 (OMIM:614742)
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2 (OMIM:614743)
PULMONARY HEMOSIDEROSIS (OMIM:178550)
Polymyositis (Orphanet:732)
RIDDLE SYNDROME (OMIM:611943)
Reactive arthritis (Orphanet:29207)
Respiratory bronchiolitis - interstitial lung disease (Orphanet:79127)
Scleroderma (Orphanet:801)
Systemic sclerosis (Orphanet:90291)