Pulmonary infiltrates

Symptom Information:

Symptom ID: HPO:0002113
Synonyms:
Pulmonic infiltration [HPO:0002113]
Lung infiltrates [Orphanet:32640]
Lung infiltration [Orphanet:32640]
Pulmonary infiltrates [OMIM:Pulmonary infiltrates]
Pulmonic infiltration [OMIM:Pulmonic infiltration]
Lung/pulmonary infiltrates [Orphanet:32640]
Lung infiltration [MedDRA:10025102]
Lung infiltration NOS [MedDRA:10025102]
Pulmonary infiltration [MedDRA:10025102]
Pulmonary infiltration NOS [MedDRA:10025102]
Bilateral alveolar infiltration [MedDRA:10025102]
Bilateral pulmonary infiltrates [MedDRA:10025102]
Pulmonary infiltration [OMIM:Pulmonary infiltration]
Quality:
Cross references:
Orphanet:32640 "Lung/pulmonary infiltrates" [Orphanet:32640]
OMIM: "Pulmonary infiltrates" [OMIM:Pulmonary infiltrates]
OMIM: "Pulmonic infiltration" [OMIM:Pulmonic infiltration]
OMIM: "Pulmonary infiltration" [OMIM:Pulmonary infiltration]
UMLS:C0235896 "Lung infiltration" [Orphanet:32640]
Is a (Direct Parents):
Orphanet Radiologic lung abnormalities/changes
MedDRA Parenchymal lung disorders NEC
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 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)
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)