Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Primary intestinal lymphangiectasia
Occasional (5-29%)
Alpha thalassaemia syndrome
Frequent (30-79%)
Johanson-Blizzard syndrome
Neu-Laxova syndrome
Frequent (30-79%)
HELLP syndrome
Frequent (30-79%)
Secondary Meig's syndrome
Occasional (5-29%)
Eisenmenger's complex
Very rare (1-4%)
Megacystis, microcolon, hypoperistalsis syndrome
Hydrops fetalis
Occasional (5-29%)
Familial haemophagocytic lymphohistiocytosis
Eisenmenger syndrome
Very rare (1-4%)
Hemorrhagic fever caused by Lujo virus
Frequent (30-79%)
Mannosyl-oligosaccharide glycosidase congenital disorder of glycosylation
Occasional (5-29%)
PIEZO1-related generalised lymphatic dysplasia with non-immune hydrops fetalis
Infection-related HUS (haemolytic uraemic syndrome)
Very rare (1-4%)
CHAPLE (complement hyperactivation, angiopathic thrombosis, protein losing enteropathy) syndrome
Quick Facts
- SNOMED CT
- 271808008
- UMLS CUI
- C1850534
- Fully Specified Name
- Generalized edema (finding)
- Associated Conditions
- 16
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.