OMOP Concept 37396000
Transthyretin related familial amyloid cardiomyopathy
StandardConditionSNOMED715655000Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Transthyretin related familial amyloid cardiomyopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| HPO | HP_0031327 | Cardiac transthyretin amyloid deposition | Non-standard |
Synonyms
Alternative names recorded for Transthyretin related familial amyloid cardiomyopathy across source vocabularies.
- amiloidosis ATTRV1221
- ATTRV122I amyloidosis
- miocardiopatía amiloide familiar relacionada con transtiretina
- miocardiopatía amiloide familiar relacionada con transtiretina (trastorno)
- Transthyretin amyloid cardiopathy
- Transthyretin related familial amyloid cardiomyopathy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(38)Roll up to these when you need a wider cohort.
- 1Cardiac familial non-neuropathic amyloidosis
- 1Cardiovascular system hereditary disorder
- 1Familial restrictive cardiomyopathy
- 1Hereditary ATTR amyloidosis
- 1Infiltrative cardiomyopathy
- 2Autosomal dominant hereditary disorder
- 2Cardiomyopathy
- 2Disorder of cardiovascular system
- 2Familial cardiomyopathy
- 2Familial non-neuropathic amyloidosis
- 2Hereditary amyloidosis
- 2Hereditary disorder by system
- 2Restrictive cardiomyopathy
- 2Structural disorder of heart
- 2Systemic amyloidosis
- 3Amyloidosis
- 3Autosomal hereditary disorder
- 3Cardiovascular finding
- 3Disorder of body system
- 3Familial disease
- 3Heart disease
- 3Hereditary disease
- 3Myocardial disease
- 3Systemic disease
- 4Cardiac finding
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