Hemoglobin Bart's hydrops syndrome

disorder

SNOMED 5300004CUI C0272005

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

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

Abnormal Hb

Very frequent (80-99%)HP:0011902

Cardiac insufficiency

Very frequent (80-99%)HP:0001635

Hydrops fetalis

Very frequent (80-99%)HP:0001789

Low number of red blood cells or hemoglobin

Very frequent (80-99%)HP:0001903

Paleness

Very frequent (80-99%)HP:0000980

Enlarged liver

Frequent (30-79%)HP:0002240

Hydramnios

Frequent (30-79%)HP:0001561

Large spleen

Frequent (30-79%)HP:0001744

Nonsyndromal hydrocephalus

Frequent (30-79%)HP:0000238

Oligohydramnios

Frequent (30-79%)HP:0001562

Swelling or irritation of membrane around heart

Occasional (5-29%)HP:0001701

Related Conditions

Alpha thalassaemia syndrome(parent)

Hydrops fetalis(parent)

Fetal anemia(parent)

Recessive hereditary disorder (autosomal)(parent)

Congenital anemia(parent)

Fetus with hereditary disease(parent)

Quick Facts

SNOMED CT: 5300004
UMLS CUI: C0272005
Fully Specified Name: Hemoglobin Bart's hydrops syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 11

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.