Qualitative platelet defects

Preferred Label : Qualitative platelet defects;

Inclusion CIM-10 : Thromboasthenia (hemorrhagic) (hereditary); Bernard-Soulier [giant platelet] syndrome; Thrombocytopathy; Grey platelet syndrome; Glanzmann's disease;

ICD-10 exclusion note : von Willebrand's disease (D68.0);

Diag associé à un acte (%) : 57.5;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D691;

UMLS CUI

C0235604;

Automatic exact mappings (from CISMeF team)
- Glanzmann's disease [MedDRA LLT]
- Glanzmann's thrombasthenia (disorder) [SNOMED CT concept]
- Gray Platelet Syndrome [NCIt concept]
- Gray platelet syndrome [ORDO Disease]
- Gray platelet syndrome (disorder) [SNOMED CT concept]
- Platelet disorder (disorder) [SNOMED CT concept]
- Thrombasthenia [MedDRA Preferred Term]
- Thrombocytopathy [MedDRA LLT]
- Thrombocytopathy [PASCAL descriptor]
- blood platelet disease [DO Concept]
- thrombasthenia [MeSH Descriptor]
Currated CISMeF NLP mapping
- Qualitative Platelet Disorder [NCIt concept]
- Qualitative platelet defects [ICD-11 Category]
- Qualitative platelet defects [ICD-9 code]
- Qualitative platelet defects [ICD-10 Sub-category (who)]
- Qualitative platelet disorder (disorder) [SNOMED CT concept]
- qualitative platelet defect [DO Concept]
- qualitative platelet disorder, nos [SNOMED Notion]
DO Cross reference
- Glanzmann's thrombasthenia [DO Concept]
- gray platelet syndrome [DO Concept]
- platelet-type bleeding disorder 17 [DO Concept]
- platelet-type bleeding disorder 18 [DO Concept]
- qualitative platelet defect [DO Concept]
ICD-10 exclusion(s)
- Von Willebrand's disease [ICD-10 Sub-category]
Orphanet concepts
- Alpha delta granule deficiency [ORDO Disease]
- Alpha granule disease [ORDO Disease]
- Bernard-Soulier syndrome [ORDO Disease]
- Bleeding disorder due to CalDAG-GEFI deficiency [ORDO Disease]
- Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder [ORDO Disease]
- Dense granule disease [ORDO Disease]
- Glanzmann thrombasthenia [ORDO Disease]
- Gray platelet syndrome [ORDO Disease]
- Isolated delta-storage pool disease [ORDO Disease]
- Isolated hereditary giant platelet disorder [ORDO Disease]
- Macrophage activation syndrome [ORDO Disease]
- Medich giant platelet syndrome [ORDO Disease]
- Mediterranean macrothrombocytopenia [ORDO Disease]
- Quebec platelet disorder [ORDO Disease]
- Rare hemorrhagic disorder due to a constitutional platelet anomaly [ORDO Disease]
- White platelet syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Qualitative platelet defects [ICD-9 code]
- qualitative platelet defect [DO Concept]
Validated automatic mappings to BTNT
- Dense granule disease [ICD-11 Subcategory]
- platelet-type bleeding disorder 17 [DO Concept]
- platelet-type bleeding disorder 18 [DO Concept]

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