Henoch-Schonlein purpura

disorder

SNOMED 191306005CUI C0034152

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.

Abdominal discomfort

Very frequent (80-99%)HP:0002027

Arthritic pain

Very frequent (80-99%)HP:0002829

Blood in urine

Very frequent (80-99%)HP:0000790

Blood spots

Very frequent (80-99%)HP:0000979

Bruising susceptibility

Very frequent (80-99%)HP:0000978

Death of digestive organ tissue due to poor blood supply

Very frequent (80-99%)HP:0005244

Inflammation of blood vessel

Very frequent (80-99%)HP:0002633

Nausea and vomiting

Very frequent (80-99%)HP:0002017

Pimple

Very frequent (80-99%)HP:0200039

Skin rash

Very frequent (80-99%)HP:0000988

Brain inflammation

Frequent (30-79%)HP:0002383

Erythema

Frequent (30-79%)HP:0010783

Inflammation of testicles

Frequent (30-79%)HP:0100796

Intermittent migraine headaches

Frequent (30-79%)HP:0002076

Joint inflammation

Frequent (30-79%)HP:0001369

Muscle pain

Frequent (30-79%)HP:0003326

Obsessive dieting

Frequent (30-79%)HP:0002039

Open skin sore

Frequent (30-79%)HP:0200042

Pyrexia

Frequent (30-79%)HP:0001945

Vascular skin abnormality

Frequent (30-79%)HP:0011276

Angiooedema

Occasional (5-29%)HP:0100665

Edema

Occasional (5-29%)HP:0000969

Epilepsy

Occasional (5-29%)HP:0001250

Episcleritis

Occasional (5-29%)HP:0100534

Flat, discolored area of skin

Occasional (5-29%)HP:0012733

Gastrointestinal haemorrhage

Occasional (5-29%)HP:0002239

Glomerulopathy

Occasional (5-29%)HP:0100820

Hives

Occasional (5-29%)HP:0001025

Muscle weakness

Occasional (5-29%)HP:0001324

Optic atrophy

Occasional (5-29%)HP:0000648

Related Conditions

Post-infective Henoch-Schonlein purpura(child)

Purpura en cocarde(child)

Autoimmune vasculitis(parent)

Small vessel vasculitis(parent)

Hypersensitivity disorder mediated by immune complex(parent)

Quick Facts

SNOMED CT: 191306005
UMLS CUI: C0034152
Fully Specified Name: Immunoglobulin A vasculitis (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.