OMOP Concept 4034813
Congenital thyroid hypoplasia
StandardConditionSNOMED237516005Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Congenital thyroid hypoplasia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 237516005 | Congenital thyroid hypoplasia | Non-standard |
Synonyms
Alternative names recorded for Congenital thyroid hypoplasia across source vocabularies.
- Congenital thyroid hypoplasia (disorder)
- hipoplasia tiroidea congénita
- hipoplasia tiroidea congénita (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of the thyroid gland
- 2Congenital anomaly of endocrine gland
- 2Congenital anomaly of neck
- 2Disorder of thyroid gland
- 3Congenital malformation
- 3Disorder of endocrine system
- 3Disorder of neck
- 3Finding of thyroid gland
- 4Congenital disease
- 4Developmental disorder
- 4Disease
- 4Disorder of body system
- 4Finding of neck region
- 5Clinical finding
- 5Disorder of fetus and/or newborn
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