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Congenital hypofibrinogenemia

disorder
SNOMED 439145006CUI C2584774

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

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.