Overview
Congenital hypofibrinogenemia 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.
Afibrinogenemia
Always present (100%)HP:0034287
Bleeding gums
Very frequent (80-99%)HP:0000225
Bleeding tendency
Very frequent (80-99%)HP:0001892
Joint swelling
Very frequent (80-99%)HP:0001386
Menometrorrhagia
Very frequent (80-99%)HP:0400008
Nasal hemorrhage
Very frequent (80-99%)HP:0000421
Abnormal umbilical stump bleeding
Frequent (30-79%)HP:0011884
Prolonged bleeding following circumcision
Frequent (30-79%)HP:0030137
Bruising susceptibility
Occasional (5-29%)HP:0000978
Cerebral hemorrhage
Occasional (5-29%)HP:0001342
Epidural hematoma
Occasional (5-29%)HP:0100310
Excessive bleeding after minor trauma
Occasional (5-29%)HP:0001934
Hematemesis
Occasional (5-29%)HP:0002248
Prolonged bleeding after dental extraction
Occasional (5-29%)HP:0006298
Ruptured spleen
Occasional (5-29%)HP:0012223
Subdural haematoma
Occasional (5-29%)HP:0100309
Low fibrinogen level
HP:0011900
Related Conditions
Quick Facts
- SNOMED CT
- 439145006
- UMLS CUI
- C2584774
- Fully Specified Name
- Congenital hypofibrinogenemia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 17
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.