OMOP Concept 4139942
Glanzmann's thrombasthenia
StandardConditionSNOMED32942005Disorder
Maps from
7
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
7 source codes normalize to Glanzmann's thrombasthenia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 139433 | Glanzmann's thrombasthenia | Non-standard |
| ICD10CN | D69.101 | Thrombasthenia (machine translation) | Non-standard |
| MeSH | D013915 | Thrombasthenia | Non-standard |
| Nebraska Lexicon | 32942005 | Hereditary haemorrhagic thrombasthenia | Non-standard |
| OXMIS | L2879G | GLANZMANN'S DISEASE | Non-standard |
| Read | D311000 | Hereditary haemorrhagic thrombasthenia | Non-standard |
| Read | D311011 | Glanzmann's syndrome | Non-standard |
Synonyms
Alternative names recorded for Glanzmann's thrombasthenia across source vocabularies.
- Glanzmann-Naegeli disorder
- Glanzmann's disease
- Glanzmann's syndrome
- Glanzmann's thrombasthenia (disorder)
- Glanzmann thromboasthenia
- Hereditary haemorrhagic thrombasthenia
- Hereditary hemorrhagic thrombasthenia
- Hereditary thromboasthenia
- Thrombasthenia
- trastorno de Glanzmann - Naegeli
- trombastenia de Glanzmann
- trombastenia de Glanzmann (trastorno)
- tromboastenia de Glanzmann
- tromboastenia hereditaria
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Hereditary platelet function disorder
- 1Platelet membrane defect
- 2Inherited platelet disorder
- 2Qualitative platelet disorder
- 3Hereditary disorder of cellular element of blood
- 3Platelet disorder
- 4Disorder of cellular component of blood
- 4Disorder of hemostatic system
- 4Hereditary disorder by system
- 5Disease
- 5Disorder of body system
- 5Finding of blood, lymphatics and immune system
- 5Functional finding
- 5Hereditary disease
- 6Clinical finding
- 6Genetic disease
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