Related Conditions
Deficiency of naturally occurring coagulation factor inhibitor(child)
Contact factor deficiency(child)
Prothrombin complex deficiency(child)
Fibrinogen abnormality(child)
Acquired coagulation disorder(child)
Blood coagulation disorder, categorized by value of screening test(child)
von Willebrand disorder(child)
Pseudo von Willebrand disease(child)
Disseminated intravascular coagulation(child)
Familial hemorrhagic diathesis(child)
Blood coagulation disorder due to liver disease(child)
Hyperheparinemia(child)
Coagulation factor deficiency syndrome(child)
Disorder of fibrinolysis(child)
Postpartum coagulation defects(child)
Blood coagulation disorder complicating childbirth(child)
Blood coagulation disorder in pregnancy(child)
Kasabach-Merritt syndrome(child)
Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency(child)
Defect of purinergic receptor p2y G protein-coupled 12(child)
Quick Facts
- SNOMED CT
- 64779008
- UMLS CUI
- C0005779
- Fully Specified Name
- Blood coagulation disorder (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
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.