OMOP Concept 4261970
Familial cardiomyopathy
StandardConditionSNOMED35728003Disorder
Maps from
3
Descendants
8
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 Familial cardiomyopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 140591 | Familial cardiomyopathy | Non-standard |
| OXMIS | 425 FM | FAMILIAL CARDIOMYOPATHY | Non-standard |
| Read | G554200 | Familial cardiomyopathy | Non-standard |
Synonyms
Alternative names recorded for Familial cardiomyopathy across source vocabularies.
- Familial cardiomyopathy (disorder)
- miocardiopatía familiar
- miocardiopatía familiar primaria
- miocardiopatía familiar (trastorno)
- Primary familial cardiomyopathy
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(20)Roll up to these when you need a wider cohort.
- 1Cardiomyopathy
- 1Familial disease
- 2Disease
- 2Myocardial disease
- 3Clinical finding
- 3Heart disease
- 3Myocardial finding
- 4Cardiac finding
- 4Disorder of cardiovascular system
- 4Disorder of mediastinum
- 5Cardiovascular finding
- 5Disorder of body system
- 5Disorder of thorax
- 5Mediastinal finding
- 5Viscus structure finding
- 6Disorder of thoracic segment of trunk
- 6Finding of region of thorax
- 7Disorder of trunk
- 7Finding of upper trunk
- 8Finding of trunk structure
Narrower concepts
(8)Included automatically when you query with descendants.
- 1Danish type familial amyloid cardiomyopathy
- 1Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
- 1Familial restrictive cardiomyopathy
- 1Primary familial dilated cardiomyopathy
- 1Primary familial hypertrophic cardiomyopathy
- 2Dilated cardiomyopathy with genetic marker
- 2Restrictive cardiomyopathy secondary to familial storage disease
- 2Transthyretin related familial amyloid cardiomyopathy
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