Upshaw-Schulman syndrome

disorder

SNOMED 373420004CUI C1268935

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.

Yellowing of the skin

Frequent (30-79%)HP:0000952

Cerebral vascular events

Occasional (5-29%)HP:0001297

Laboured breathing

Occasional (5-29%)HP:0002098

Transient ischemic attacks

Occasional (5-29%)HP:0002326

Myocardial infarction

Very rare (1-4%)HP:0001658

Confusion

HP:0001289

Hemolytic-uremic syndrome

HP:0005575

Higher than normal levels of lactate in blood

HP:0002151

Increased blood urea nitrogen

HP:0003138

Increased creatinine

HP:0003259

Low platelet count

HP:0001873

Microangiopathic hemolytic anemia

HP:0001937

Microhematuria

HP:0002907

Prolonged neonatal jaundice

HP:0006579

Proteinuria

HP:0000093

Pyrexia

HP:0001945

Renal functional abnormality

HP:0012211

Reticulocytosis

HP:0001923

Schistocytes

HP:0001981

Tremor

HP:0001337

Related Conditions

Thrombotic thrombocytopenic purpura(parent)

Hereditary red blood cell disorder(parent)

Cardiovascular system hereditary disorder(parent)

Inherited platelet disorder(parent)

Hereditary disorder of the integument(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 373420004
UMLS CUI: C1268935
Fully Specified Name: Upshaw-Schulman syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 20

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.