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Heparin cofactor II deficiency

disorder
SNOMED 234468009CUI C0398626

Overview

Heparin cofactor II deficiency 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.

Disseminated intravascular coagulation
HP:0005521
Post-angioplasty coronary artery restenosis
HP:0004761
Recurrent venous thrombosis
HP:0004850

Quick Facts

SNOMED CT
234468009
UMLS CUI
C0398626
Fully Specified Name
Heparin cofactor II deficiency (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
3
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.