Overview
Hereditary factor XIII A subunit 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.
Abnormal umbilical stump bleeding
Always present (100%)HP:0011884
Bleeding gums
Always present (100%)HP:0000225
Bleeding tendency
Always present (100%)HP:0001892
Bruising susceptibility
Always present (100%)HP:0000978
Ecchymosis
Always present (100%)HP:0031364
Reduced factor XIII activity
Always present (100%)HP:0008357
Reduced factor XIII, subunit A
Always present (100%)HP:0040233
Excessive bleeding after minor trauma
Frequent (30-79%)HP:0001934
Spontaneous hematomas
Frequent (30-79%)HP:0007420
Intracranial haemorrhage
HP:0002170
Joint hemorrhage
HP:0005261
Nasal hemorrhage
HP:0000421
Related Conditions
Quick Facts
- SNOMED CT
- 439455002
- UMLS CUI
- C2750514
- Fully Specified Name
- Hereditary factor XIII A subunit deficiency (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 12
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.