OMOP Concept 437241
Qualitative platelet disorder
StandardConditionSNOMED267532001Disorder
Maps from
15
Descendants
32
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
15 source codes normalize to Qualitative platelet disorder via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 110861 | Thrombocytopathy | Non-standard |
| CIEL | 127975 | Qualitative platelet defect | Non-standard |
| CIM10 | D69.1 | Qualitative platelet defects | Non-standard |
| ICD10 | D69.1 | Qualitative platelet defects | Non-standard |
| ICD10CM | D69.1 | Qualitative platelet defects | Non-standard |
| ICD10CN | D69.1 | Qualitative platelet defects | Non-standard |
| ICD10CN | D69.100 | Qualitative platelet defects | Non-standard |
| ICD10CN | D69.102 | Bernard-Soulier syndrome (machine translation) | Non-standard |
| ICD10CN | D69.103 | Gray platelet syndrome (machine translation) | Non-standard |
| ICD10GM | D69.1 | Qualitative platelet defects | Non-standard |
| ICD9CM | 287.1 | Qualitative platelet defects | Non-standard |
| KCD7 | D69.1 | Qualitative platelet defects | Non-standard |
| Nebraska Lexicon | 267532001 | Qualitative platelet disorder | Non-standard |
| Read | D311.00 | Qualitative platelet defects | Non-standard |
| Read | D311z00 | Qualitative platelet deficiency NOS | Non-standard |
Synonyms
Alternative names recorded for Qualitative platelet disorder across source vocabularies.
- Qualitative platelet defect
- Qualitative platelet disorder (disorder)
- trastorno plaquetario cualitativo
- trastorno plaquetario cualitativo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(7)Roll up to these when you need a wider cohort.
Narrower concepts
(32)Included automatically when you query with descendants.
- 1Acquired platelet function disorder
- 1Hereditary platelet function disorder
- 2Bernard Soulier syndrome
- 2Bleeding diathesis due to collagen receptor defect
- 2Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency
- 2Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
- 2Defect of purinergic receptor p2y G protein-coupled 12
- 2Familial alpha-2 adrenergic receptor defect in platelets
- 2Glanzmann's thrombasthenia
- 2Isolated collagen aggregation defect
- 2Platelet dysfunction associated with uremia
- 2Platelet dysfunction caused by aspirin
- 2Platelet procoagulant activity deficiency
- 2Platelet secretory disorder
- 2Platelet storage pool defect
- 2Pseudo von Willebrand disease
- 2Scott syndrome
- 2Severe autosomal recessive macrothrombocytopenia
- 3Autosomal dominant thrombocytopenia with platelet secretion defect
- 3Dense body defect
- 3Gray platelet syndrome
- 3Mixed alpha granule and dense body deficiency
- 3Platelet factor V deficiency (factor V Quebec)
- 3White platelet syndrome
- 4Chédiak-Higashi syndrome
- 4Familial platelet syndrome with predisposition to acute myelogenous leukemia
- 4Hermansky-Pudlak syndrome
- 4Medich giant platelet syndrome
- 4Platelet dense granule deficiency
- 4Wiskott-Aldrich syndrome
- 5Attenuated Chédiak-Higashi syndrome
- 5Wiskott-Aldrich autosomal dominant variant syndrome
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