OMOP Concept 133728
Congenital hypothyroidism
StandardConditionSNOMED190268003Disorder
Maps from
9
Descendants
55
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
9 source codes normalize to Congenital hypothyroidism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 143893 | Congenital hypothyroidism | Non-standard |
| HPO | HP_0000851 | Congenital hypothyroidism | Non-standard |
| ICD9CM | 243 | Congenital hypothyroidism | Non-standard |
| MeSH | D003409 | Congenital Hypothyroidism | Non-standard |
| Nebraska Lexicon | 190268003 | Congenital hypothyroidism | Non-standard |
| Read | C03..00 | Congenital hypothyroidism | Non-standard |
| Read | C03y.00 | Other specified congenital hypothyroidism | Non-standard |
| Read | C03z.00 | Congenital hypothyroidism NOS | Non-standard |
| Read | C03z.11 | Congenital thyroid insufficiency | Non-standard |
Synonyms
Alternative names recorded for Congenital hypothyroidism across source vocabularies.
- Congenital hypothyroidism (disorder)
- hipotiroidismo congénito
- hipotiroidismo congénito (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(11)Roll up to these when you need a wider cohort.
Narrower concepts
(55)Included automatically when you query with descendants.
- 1Athyrotic hypothyroidism sequence
- 1Bamforth Lazarus syndrome
- 1Congenital central hypothyroidism
- 1Congenital hypothyroidism due to absence of thyroid gland
- 1Congenital hypothyroidism due to congenital anomaly of thyroid gland
- 1Congenital hypothyroidism due to dual oxidase maturation factor 2
- 1Congenital hypothyroidism due to iodine deficiency
- 1Congenital hypothyroidism due to maternal intake of antithyroid drug
- 1Congenital hypothyroidism due to peripheral resistance to thyroid hormone
- 1Congenital hypothyroidism due to symporter mutation
- 1Congenital hypothyroidism due to thyroglobulin mutation
- 1Congenital hypothyroidism due to thyroid deiodinase mutation
- 1Congenital hypothyroidism due to thyroid peroxidase mutation
- 1Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody
- 1Congenital hypothyroidism with diffuse goiter
- 1Congenital hypothyroidism without goiter
- 1Dyshormonogenic goiter
- 1Familial thyroid dyshormonogenesis
- 1Genetic transient congenital hypothyroidism
- 1Hypothyroidism due to defect in thyroid hormone synthesis
- 1Hypothyroidism due to iodide trapping defect
- 1Hypothyroidism due to mutation in transcription factor of pituitary development
- 1Idiopathic congenital hypothyroidism
- 1Iodide oxidation defect
- 1Iodide transport defect
- 1Myxedematous form of cretinism
- 1Neonatal jaundice with congenital hypothyroidism
- 1Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome
- 1Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant
- 1Resistance to thyroid hormone due to mutation in thyroid hormone receptor alpha
- 1Short stature with delayed bone age due to thyroid hormone metabolism deficiency
- 1Sporadic cretinism
- 1Thyroid hormone responsiveness defect
- 1Transient congenital hypothyroidism due to dual oxidase 2 mutation
- 2Allan-Herndon-Dudley syndrome
- 2Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency
- 2Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation
- 2Congenital malposition of the thyroid gland
- 2Dyshormonogenetic goiter AND iodide leak
- 2Endemic congenital iodine deficiency syndrome of myxedematous type
- 2Familial dyshormonogenetic goiter
- 2Hypothyroidism due to iodide organification defect
- 2Iodotyrosine deiodination defect
- 2Iodotyrosyl coupling defect
- 2Peripheral resistance to thyroid hormone
- 2Thyroglobulin synthesis defect
- 2Thyroid hormone resistance syndrome
- 3Congenital iodine deficiency syndrome of mixed type
- 3Generalized thyroid hormone resistance
- 3Pituitary thyroid hormone resistance
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