Parkes Weber syndrome

disorder

SNOMED 234143003CUI C5574870

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.

Abnormality of the lower limb

Very frequent (80-99%)HP:0002814

Arteriovenous malformation

Very frequent (80-99%)HP:0100026

Arteriovenous fistula

Frequent (30-79%)HP:0004947

Bounding pulse

Frequent (30-79%)HP:0032555

Capillary malformation

Frequent (30-79%)HP:0025104

Erythematous plaque

Frequent (30-79%)HP:0025474

High-output congestive heart failure

Frequent (30-79%)HP:0001722

Muscle hypertrophy of the lower extremities

Frequent (30-79%)HP:0008968

Overgrowth of one leg

Frequent (30-79%)HP:0100553

Peripheral arteriovenous fistula

Frequent (30-79%)HP:0100784

Prominent superficial vasculature

Frequent (30-79%)HP:0007394

Twisted blood vessels

Frequent (30-79%)HP:0004948

Varicose veins

Frequent (30-79%)HP:0002619

Venous malformations

Frequent (30-79%)HP:0012721

Wider than typical opening or gap

Frequent (30-79%)HP:0002617

Abnormal circulating B-type natriuretic peptide concentration

Occasional (5-29%)HP:0031138

Abnormal lymphatic vessel morphology

Occasional (5-29%)HP:0100766

Abnormality of the arm

Occasional (5-29%)HP:0002817

Abnormality of the urinary system

Occasional (5-29%)HP:0000079

Abnormality of the wide portion of the femoral bone

Occasional (5-29%)HP:0006489

Back pain

Occasional (5-29%)HP:0003418

Bleeding tendency

Occasional (5-29%)HP:0001892

Cerebral AV malformation

Occasional (5-29%)HP:0002408

Chest pain

Occasional (5-29%)HP:0100749

Conus terminalis arteriovenous malformation

Occasional (5-29%)HP:0031939

Disseminated intravascular coagulation

Occasional (5-29%)HP:0005521

Dural ectasia

Occasional (5-29%)HP:0100775

Headache

Occasional (5-29%)HP:0002315

Increased size of upper limb

Occasional (5-29%)HP:0010484

Loss of distal sensation

Occasional (5-29%)HP:0002936

Related Conditions

Angio-osteohypertrophic syndrome(parent)

Quick Facts

SNOMED CT: 234143003
UMLS CUI: C5574870
Fully Specified Name: Parkes Weber 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.