Treatments & Interventions
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal platelet function
Very frequent (80-99%)HP:0011869
Abnormality of coagulation
Very frequent (80-99%)HP:0001928
Platelet abnormalities
Very frequent (80-99%)HP:0001872
Reduced von Willebrand factor activity
Very frequent (80-99%)HP:0008330
Abnormal mitral valve morphology
Frequent (30-79%)HP:0001633
Bruising susceptibility
Frequent (30-79%)HP:0000978
Factor VIII deficiency
Frequent (30-79%)HP:0003125
Gastrointestinal angiodysplasia
Frequent (30-79%)HP:0000471
Hypermenorrhea
Frequent (30-79%)HP:0000132
Impaired ristocetin cofactor assay activity
Frequent (30-79%)HP:0030129
Nasal hemorrhage
Frequent (30-79%)HP:0000421
Finger pointing in a different direction than usual
Occasional (5-29%)HP:0004097
Gastrointestinal haemorrhage
Occasional (5-29%)HP:0002239
Intramuscular hemorrhage
Occasional (5-29%)HP:0040242
Joint hemorrhage
Occasional (5-29%)HP:0005261
Microcytic anemia
Occasional (5-29%)HP:0001935
Petechiae
Occasional (5-29%)HP:0000967
Prolonged activated partial thromboplastin time
Occasional (5-29%)HP:0003645
Thrombocytopenia
Occasional (5-29%)HP:0001873
Venous insufficiency
Occasional (5-29%)HP:0005293
Increased bleeding time
HP:0003010
Intermittent thrombocytopenia
HP:0004854
Quick Facts
- SNOMED CT
- 128105004
- UMLS CUI
- C0042974
- Fully Specified Name
- von Willebrand disorder (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 22
- Known Treatments
- 10
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.