Overview
Congenital alpha-2-antiplasmin 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.
Excessive bleeding after minor trauma
Very frequent (80-99%)HP:0001934
Joint hemorrhage
Very frequent (80-99%)HP:0005261
Bleeding tendency
Frequent (30-79%)HP:0001892
Blood in urine
Frequent (30-79%)HP:0000790
Hemothorax
Frequent (30-79%)HP:0012151
Intramuscular haematoma
Frequent (30-79%)HP:0012233
Reduced euglobulin clot lysis time
Frequent (30-79%)HP:0040247
Abnormal umbilical stump bleeding
Occasional (5-29%)HP:0011884
Bleeding gums
Occasional (5-29%)HP:0000225
Bone pain
Occasional (5-29%)HP:0002653
Bruising susceptibility
Occasional (5-29%)HP:0000978
Intracranial haemorrhage
Occasional (5-29%)HP:0002170
Quick Facts
- SNOMED CT
- 716746003
- UMLS CUI
- C4274304
- Fully Specified Name
- Congenital alpha-2-antiplasmin 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.