Pulmonary fibrosis
Symptom Information:
Symptom ID: | HPO:0002206 | |||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |