Overview
Hereditary platelet function disorder is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Scott syndrome(child)
Platelet storage pool defect(child)
Familial alpha>2< adrenergic receptor defect in platelets(child)
Isolated collagen aggregation defect(child)
Hereditary thromboasthenia(child)
Platelet procoagulant activity deficiency(child)
Platelet secretory disorder(child)
Bernard Soulier syndrome(child)
Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency(child)
Defect of purinergic receptor p2y G protein-coupled 12(child)
Bleeding diathesis due to collagen receptor defect(child)
PLA2G4A (phospholipase A2 group IVA) related platelet dysfunction(child)
Severe autosomal recessive macrothrombocytopenia(child)
Pseudo von Willebrand disease(child)
Inherited platelet disorder(parent)
Qualitative platelet defect(parent)
Quick Facts
- SNOMED CT
- 128096008
- UMLS CUI
- C1264033
- Fully Specified Name
- Hereditary platelet function disorder (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
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.