Overview
Hereditary factor XIII type I deficiency is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Quick Facts
- SNOMED CT
- 439460003
- UMLS CUI
- C2585089
- Fully Specified Name
- Hereditary factor XIII A subunit and B subunit deficiency (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.