OMOP Concept 4027376
Platelet storage pool defect
StandardConditionSNOMED128099001Disorder
Maps from
3
Descendants
12
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Platelet storage pool defect via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 125854 | Storage Pool Disease of Platelets | Non-standard |
| MeSH | D010981 | Platelet Storage Pool Deficiency | Non-standard |
| Nebraska Lexicon | 128099001 | Platelet storage organelle defect | Non-standard |
Synonyms
Alternative names recorded for Platelet storage pool defect across source vocabularies.
- defecto en el almacenamiento de plaquetas
- defecto en el almacenamiento de plaquetas (trastorno)
- defecto en las organelas de almacenamiento de las plaquetas
- Platelet storage organelle defect
- Platelet storage pool defect (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(17)Roll up to these when you need a wider cohort.
- 1Congenital disease
- 1Hereditary platelet function disorder
- 2Disorder of fetus and/or newborn
- 2Inherited platelet disorder
- 2Qualitative platelet disorder
- 3Disease
- 3Hereditary disorder of cellular element of blood
- 3Platelet disorder
- 4Clinical finding
- 4Disorder of cellular component of blood
- 4Disorder of hemostatic system
- 4Hereditary disorder by system
- 5Disorder of body system
- 5Finding of blood, lymphatics and immune system
- 5Functional finding
- 5Hereditary disease
- 6Genetic disease
Narrower concepts
(12)Included automatically when you query with descendants.
- 1Dense body defect
- 1Gray platelet syndrome
- 1Mixed alpha granule and dense body deficiency
- 1White platelet syndrome
- 2Chédiak-Higashi syndrome
- 2Familial platelet syndrome with predisposition to acute myelogenous leukemia
- 2Hermansky-Pudlak syndrome
- 2Medich giant platelet syndrome
- 2Platelet dense granule deficiency
- 2Wiskott-Aldrich syndrome
- 3Attenuated Chédiak-Higashi syndrome
- 3Wiskott-Aldrich autosomal dominant variant syndrome
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