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Hydrops fetalis

disorder
SNOMED 276508000CUI C0020305

Overview

Hydrops fetalis is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Ascites
Frequent (30-79%)HP:0001541
Birth weight less than 10th percentile
Frequent (30-79%)HP:0001518
Deformity of the neck
Frequent (30-79%)HP:0000464
Increased placental thickness
Frequent (30-79%)HP:0032548
Nonimmune hydrops fetalis
Frequent (30-79%)HP:0001790
Systemic capillary leak syndrome
Frequent (30-79%)HP:0030005
Abnormality of cardiovascular system morphology
Occasional (5-29%)HP:0030680
Fluid around lungs
Occasional (5-29%)HP:0002202
Generalised oedema
Occasional (5-29%)HP:0007430
Hematological abnormality
Occasional (5-29%)HP:0001871
Hydramnios
Occasional (5-29%)HP:0001561
Lymphoedema
Occasional (5-29%)HP:0001004
Pericardial effusions
Occasional (5-29%)HP:0001698
Renal anomalies
Occasional (5-29%)HP:0000077
Unusual course of infection
Occasional (5-29%)HP:0032169
Abnormal heart rate
Very rare (1-4%)HP:0011675
Abnormal skeletal development
Very rare (1-4%)HP:0002652
Abnormality of the urinary system
Very rare (1-4%)HP:0000079
Cardiac anomaly
Very rare (1-4%)HP:0001627
Gastrointestinal disease
Very rare (1-4%)HP:0011024
Lymphatic disease
Very rare (1-4%)HP:0100763
Oncology
Very rare (1-4%)HP:0002664
Twin-to-twin transfusion
Very rare (1-4%)HP:0031110

Quick Facts

SNOMED CT
276508000
UMLS CUI
C0020305
Fully Specified Name
Hydrops fetalis (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
23
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.