Pulmonary infiltrates
Symptom Information:
Symptom ID: | HPO:0002113 | |||||||||||||
Synonyms: |
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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 infiltrates(HPO:0002113) 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 infiltrates(HPO:0002113) |
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Database Frequency: | 36 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
Acute interstitial pneumonia | (Orphanet:79126) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Alveolar echinococcosis | (Orphanet:284) |
Anti-glomerular basement membrane disease | (Orphanet:375) |
Behçet disease | (Orphanet:117) |
Bronchiolitis obliterans with obstructive pulmonary disease | (Orphanet:1303) |
Cogan syndrome | (Orphanet:1467) |
Cryptogenic organizing pneumonia | (Orphanet:1302) |
Desquamative interstitial pneumonia | (Orphanet:98852) |
Drug rash with eosinophilia and systemic symptoms | (Orphanet:139402) |
Eosinophilic granuloma | (Orphanet:99871) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Gaucher disease type 1 | (Orphanet:77259) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Griscelli disease type 2 | (Orphanet:79477) |
HISTIOCYTOSIS, FAMILIAL LIPOCHROME | (OMIM:235900) |
Hand-Schüller-Christian disease | (Orphanet:99873) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Idiopathic acute eosinophilic pneumonia | (Orphanet:724) |
Idiopathic hypereosinophilic syndrome | (Orphanet:3260) |
Idiopathic pulmonary fibrosis | (Orphanet:2032) |
Legionellosis | (Orphanet:549) |
Letterer-Siwe disease | (Orphanet:99870) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Lymphoid interstitial pneumonia | (Orphanet:79128) |
Majeed syndrome | (Orphanet:77297) |
Non-specific interstitial pneumonia | (Orphanet:91364) |
Pulmonary capillary hemangiomatosis | (Orphanet:199241) |
Pulmonary venoocclusive disease | (Orphanet:31837) |
Pyoderma gangrenosum | (Orphanet:48104) |
Pyruvate dehydrogenase lipoic acid synthetase deficiency | (OMIM:614462) |
Respiratory bronchiolitis - interstitial lung disease | (Orphanet:79127) |
Scleroderma | (Orphanet:801) |
Sea-blue histiocytosis | (Orphanet:158029) |
Sweet syndrome | (Orphanet:3243) |
Waldenström macroglobulinemia | (Orphanet:33226) |