von Willebrand disease type 3

disorder

SNOMED 128108002CUI C1264041

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.

Factor VIII deficiency

Always present (100%)HP:0003125

Reduced von Willebrand factor activity

Always present (100%)HP:0008330

Joint hemorrhage

Occasional (5-29%)HP:0005261

Bleeding tendency

HP:0001892

Bruising susceptibility

HP:0000978

Excessive bleeding after minor trauma

HP:0001934

Frequent nosebleeds

HP:0000421

Hypermenorrhea

HP:0000132

Impaired platelet aggregation

HP:0003540

Increased bleeding time

HP:0003010

Low platelet count

HP:0001873

Protracted bleeding after surgery

HP:0004846

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Hereditary von Willebrand disease(parent)

Quick Facts

SNOMED CT: 128108002
UMLS CUI: C1264041
Fully Specified Name: Hereditary von Willebrand disease type 3 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

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.