Acquired von Willebrand's disease

disorder

SNOMED 234451005CUI C0272362

Overview

Acquired von Willebrand's disease is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Abnormality of cardiovascular system morphology

Frequent (30-79%)HP:0030680

Blood tumor

Frequent (30-79%)HP:0004377

Factor VIII deficiency

Frequent (30-79%)HP:0003125

Impaired ristocetin cofactor assay activity

Frequent (30-79%)HP:0030129

Low factor II activity

Frequent (30-79%)HP:0008151

Reduced von Willebrand factor activity

Frequent (30-79%)HP:0008330

Abnormal uterus bleeding

Occasional (5-29%)HP:0100608

Aortic stenosis

Occasional (5-29%)HP:0001650

Aortic valve regurgitation

Occasional (5-29%)HP:0001659

Black faeces

Occasional (5-29%)HP:0002249

Bleeding below the skin

Occasional (5-29%)HP:0001933

Bruising susceptibility

Occasional (5-29%)HP:0000978

Excessive bleeding after minor trauma

Occasional (5-29%)HP:0001934

Gastrointestinal angiodysplasia

Occasional (5-29%)HP:0000471

Gastrointestinal haemorrhage

Occasional (5-29%)HP:0002239

High urine occult blood

Occasional (5-29%)HP:0000790

Hypermenorrhea

Occasional (5-29%)HP:0000132

Hypochromic anemia

Occasional (5-29%)HP:0001931

Hypotension

Occasional (5-29%)HP:0002615

Joint hemorrhage

Occasional (5-29%)HP:0005261

Mitral regurgitation, mild

Occasional (5-29%)HP:0001653

Nasal hemorrhage

Occasional (5-29%)HP:0000421

Normocytic anemia

Occasional (5-29%)HP:0001897

Prostration

Occasional (5-29%)HP:0025406

Pulmonary stenosis

Occasional (5-29%)HP:0001642

Refractory anemia

Occasional (5-29%)HP:0005505

Intracranial haemorrhage

Very rare (1-4%)HP:0002170

Related Conditions

von Willebrand factor inhibitor disorder(child)

von Willebrand disorder(parent)

Acquired coagulation disorder(parent)

Quick Facts

SNOMED CT: 234451005
UMLS CUI: C0272362
Fully Specified Name: Acquired von Willebrand disease (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 27

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.