HELLP syndrome

disorder

SNOMED 95605009CUI C0162739

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.

Elevated serum transaminases

Always present (100%)HP:0002910

Thrombocytopenia

Always present (100%)HP:0001873

Hemolytic anaemia

Very frequent (80-99%)HP:0001878

Generalised oedema

Frequent (30-79%)HP:0007430

Headache

Frequent (30-79%)HP:0002315

Increased body weight

Frequent (30-79%)HP:0004324

Low factor II activity

Frequent (30-79%)HP:0008151

Low fibrinogen level

Frequent (30-79%)HP:0011900

Proteinuria

Frequent (30-79%)HP:0000093

Tiredness

Frequent (30-79%)HP:0012378

Back pain

Occasional (5-29%)HP:0003418

Decreased mean corpuscular haemoglobin

Occasional (5-29%)HP:0025547

Disseminated intravascular coagulation

Occasional (5-29%)HP:0005521

Epigastrium pain

Occasional (5-29%)HP:0410019

Excess fluid in lungs

Occasional (5-29%)HP:0100598

Fluid around lungs

Occasional (5-29%)HP:0002202

Hemoglobinuria

Occasional (5-29%)HP:0003641

Hypotension

Occasional (5-29%)HP:0002615

Increased lactate dehydrogenase level

Occasional (5-29%)HP:0025435

Microangiopathic hemolytic anemia

Occasional (5-29%)HP:0001937

Nausea

Occasional (5-29%)HP:0002018

Placental abruption

Occasional (5-29%)HP:0011419

Poor wound healing

Occasional (5-29%)HP:0001058

Shoulder pain

Occasional (5-29%)HP:0030834

Upset stomach

Occasional (5-29%)HP:0002027

Vomiting

Occasional (5-29%)HP:0002013

Acute kidney failure

Very rare (1-4%)HP:0001919

Cerebral hemorrhage

Very rare (1-4%)HP:0001342

Internal bleeding

Very rare (1-4%)HP:0011029

Edema

HP:0000969

Related Conditions

Postpartum hemolysis-elevated liver enzymes-low platelet count syndrome(child)

Severe pre-eclampsia(parent)

Acquired thrombocytopenia(parent)

Quick Facts

SNOMED CT: 95605009
UMLS CUI: C0162739
Fully Specified Name: Hemolysis-elevated liver enzymes-low platelet count syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.