OMOP Concept 4094599
Autosomal variant form of transthyretin
StandardConditionSNOMED25067009Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Autosomal variant form of transthyretin via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 148079 | Autosomal variant form of transthyretin | Non-standard |
| Nebraska Lexicon | 25067009 | Autosomal variant form of transthyretin | Non-standard |
Synonyms
Alternative names recorded for Autosomal variant form of transthyretin across source vocabularies.
- Autosomal variant form of transthyretin (disorder)
- forma variante de transtirretina, autosómica
- forma variante de transtirretina, autosómica (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
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