Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Severe hemophilia A
Occasional (5-29%)
Glucose-6-phosphate transport defect
Occasional (5-29%)
Hereditary thromboasthenia
Occasional (5-29%)
Hereditary factor II deficiency disease
Factor VII deficiency
Frequent (30-79%)
Hereditary factor XI deficiency disease
Frequent (30-79%)
Hereditary factor XIII deficiency disease
Occasional (5-29%)
Gray platelet syndrome
Bernard Soulier syndrome
Frequent (30-79%)
Factor X deficiency
Occasional (5-29%)
Hereditary factor V deficiency disease
Scott syndrome
Occasional (5-29%)
von Willebrand disorder
Frequent (30-79%)
von Willebrand disease type 1
von Willebrand disease type 2
von Willebrand disease type 3
Acquired von Willebrand's disease
Occasional (5-29%)
Giant platelet syndrome
Frequent (30-79%)
Hyperprolactinemia
Frequent (30-79%)
Gardner-Diamond syndrome
Occasional (5-29%)
Hereditary von Willebrand disease type 2A
Hereditary von Willebrand disease type 2B
von Willebrand disease type 2N
Fowler's syndrome
Very rare (1-4%)
MYH9 related disease
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 386692008
- UMLS CUI
- C0025323
- Fully Specified Name
- Menorrhagia (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.