Pulmonary edema

Symptom Information:

Symptom ID: HPO:0100598
Synonyms:
Pulmonary edema (disorder) [Orphanet:32720]
Pulmonary Edema [Orphanet:32720]
Pulmonary edema [Orphanet:32720]
Pulmonary oedema [Orphanet:32720]
Pulmonary oedema [MedDRA:10037423]
Edema lung [MedDRA:10037423]
Edema pulmonary [MedDRA:10037423]
Lung edema [MedDRA:10037423]
Lung oedema [MedDRA:10037423]
Oedema pulmonary [MedDRA:10037423]
Pulmonary edema [MedDRA:10037423]
Pulmonary edema cardiac cause [MedDRA:10037423]
Pulmonary oedema cardiac cause [MedDRA:10037423]
Pulmonary oedema NOS [MedDRA:10037423]
Pulmonary oedema aggravated [MedDRA:10037423]
Pulmonary edema aggravated [MedDRA:10037423]
Oedema lung [MedDRA:10037423]
Pulmonary edema recurrent [MedDRA:10037423]
Pulmonary oedema recurrent [MedDRA:10037423]
Subacute pulmonary edema [MedDRA:10037423]
Subacute pulmonary oedema [MedDRA:10037423]
Alveolar oedema [MedDRA:10037423]
Alveolar edema [MedDRA:10037423]
Lung edema [OMIM:Lung edema]
Pulmonary oedemas [MedDRA:10037424]
Quality:
Cross references:
Orphanet:32720 "Pulmonary edema" [Orphanet:32720]
OMIM: "Lung edema" [OMIM:Lung edema]
UMLS:C0034063 "Pulmonary Edema" [Orphanet:32720]
Is a (Direct Parents):
Orphanet Abnormality of the diaphragm
MedDRA Lower respiratory tract disorders (excl obstruction and infection)
HPO         Edema
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 edema(HPO:0100598)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of fluid regulation(HPO:0011032)
             Edema(HPO:0000969)
                Pulmonary edema(HPO:0100598)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Lower respiratory tract disorders (excl obstruction and infection)(MedDRA:10024967)
       Pulmonary edema(HPO:0100598)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

Acute interstitial pneumonia (Orphanet:79126)
Bronchiolitis obliterans with obstructive pulmonary disease (Orphanet:1303)
Cardiomyopathy, dilated, 1Q (OMIM:609915)
Cardiomyopathy, familial restrictive, 1 (OMIM:115210)
Familial atrial myxoma (Orphanet:615)
Familial short QT syndrome (Orphanet:51083)
Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease (Orphanet:439854)
Infant acute respiratory distress syndrome (Orphanet:70587)
Left ventricular noncompaction 10 (OMIM:615396)
Non-histaminic angioedema (Orphanet:658)
Non-specific interstitial pneumonia (Orphanet:91364)
PULMONARY EDEMA OF MOUNTAINEERS, SUSCEPTIBILITY TO (OMIM:178400)
Pulmonary capillary hemangiomatosis (Orphanet:199241)
Pulmonary venoocclusive disease (Orphanet:31837)
Systemic capillary leak syndrome (Orphanet:188)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
[DEL] GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL (OMIM:261740)