OMOP Concept 4282164
Autosomal dominant excess of transthyretin
StandardConditionSNOMED66185005Disorder
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 dominant excess of transthyretin via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 148095 | Autosomal dominant excess of transthyretin | Non-standard |
| Nebraska Lexicon | 66185005 | Autosomal dominant excess of thyroxine-binding prealbumin | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant excess of transthyretin across source vocabularies.
- Autosomal dominant excess of thyroxine-binding prealbumin
- Autosomal dominant excess of transthyretin (disorder)
- exceso autosómico dominante de globulina ligadora de tiroxina
- exceso de transtirretina autosómico dominante
- exceso de transtirretina autosómico dominante (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Thyroxine transport defect
- 2Autosomal hereditary disorder
- 2Inherited disorder of thyroid metabolism
- 3Disorder of thyroid gland
- 3Hereditary disease
- 3Hereditary disorder of endocrine system
- 3Inborn error of metabolism
- 4Congenital disease
- 4Disorder of endocrine system
- 4Disorder of neck
- 4Finding of thyroid gland
- 4Genetic disease
- 4Hereditary disorder by system
- 4Hereditary metabolic disease
- 5Disease
- 5Disorder of body system
- 5Disorder of fetus and/or newborn
- 5Finding of neck region
- 5Metabolic disease
- 6Clinical finding
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