Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Lupus anticoagulant disorder
Frequent (30-79%)
Babesiosis
Occasional (5-29%)
Antiphospholipid syndrome
Frequent (30-79%)
Stress polycythemia
Very frequent (80-99%)
Hereditary spherocytosis
Frequent (30-79%)
Deficiency of cytochrome-b>5< reductase
Frequent (30-79%)
Macroglobulinaemia
Frequent (30-79%)
Waldenstrom's macroglobulinemia
Frequent (30-79%)
Beta thalassemia intermedia
Frequent (30-79%)
Eisenmenger's complex
Very rare (1-4%)
Idiopathic livedo reticularis with summer ulceration
Frequent (30-79%)
Idiopathic hypereosinophilic syndrome
Frequent (30-79%)
Eisenmenger syndrome
Very rare (1-4%)
Klippel Trenaunay syndrome
Occasional (5-29%)
Congenital methemoglobinemia due to NADH-cytochrome b5 reductase 3 deficiency
Frequent (30-79%)
Secondary non-traumatic avascular necrosis
Very rare (1-4%)
THBD (thrombomodulin) related bleeding disorder
Acquired protein C deficiency
Idiopathic steroid-resistant nephrotic syndrome
Frequent (30-79%)
Secondary steroid-resistant nephrotic syndrome
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 76612001
- UMLS CUI
- C0398623
- Fully Specified Name
- Hypercoagulability state (finding)
- Associated Conditions
- 20
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.