OMOP Concept 140673
Hypothyroidism
StandardConditionSNOMED40930008Disorder
Maps from
36
Descendants
124
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
36 source codes normalize to Hypothyroidism via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Hypothyroidism across source vocabularies.
- hipotiroidismo
- hipotiroidismo (trastorno)
- Hypothyroid
- Hypothyroidism (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(8)Roll up to these when you need a wider cohort.
Narrower concepts
(124)Included automatically when you query with descendants.
- 1Acquired hypothyroidism
- 1Central hypothyroidism
- 1Congenital hypothyroidism
- 1Hoffman syndrome
- 1Hypothyroid dwarfism
- 1Hypothyroidism caused by radiation
- 1Hypothyroidism in childbirth
- 1Hypothyroidism in pregnancy
- 1Infant hypothyroidism
- 1Lithium induced hypothyroidism
- 1Myxedema
- 1Postpartum hypothyroidism
- 1Primary hypothyroidism
- 1Secondary hypothyroidism
- 1Severe hypothyroidism
- 1Subclinical hypothyroidism
- 1Transient hypothyroidism
- 2Acquired central hypothyroidism
- 2Adult myxedema
- 2Athyrotic hypothyroidism sequence
- 2Autoimmune hypothyroidism
- 2Bamforth Lazarus syndrome
- 2Congenital central hypothyroidism
- 2Congenital hypothyroidism due to absence of thyroid gland
- 2Congenital hypothyroidism due to congenital anomaly of thyroid gland
- 2Congenital hypothyroidism due to dual oxidase maturation factor 2
- 2Congenital hypothyroidism due to iodine deficiency
- 2Congenital hypothyroidism due to maternal intake of antithyroid drug
- 2Congenital hypothyroidism due to peripheral resistance to thyroid hormone
- 2Congenital hypothyroidism due to symporter mutation
- 2Congenital hypothyroidism due to thyroglobulin mutation
- 2Congenital hypothyroidism due to thyroid deiodinase mutation
- 2Congenital hypothyroidism due to thyroid peroxidase mutation
- 2Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody
- 2Congenital hypothyroidism with diffuse goiter
- 2Congenital hypothyroidism without goiter
- 2Consumptive hypothyroidism caused by type 3 iodothyronine deiodinase
- 2Dementia due to acquired hypothyroidism
- 2Dyshormonogenic goiter
- 2Euthyroid with thyroid antibodies
- 2Familial thyroid dyshormonogenesis
- 2Genetic transient congenital hypothyroidism
- 2Hypothalamic hypothyroidism
- 2Hypothyroid goiter, acquired
- 2Hypothyroidism caused by drug
- 2Hypothyroidism caused by food stuff
- 2Hypothyroidism caused by iodide excess
- 2Hypothyroidism due to and following radiotherapy
- 2Hypothyroidism due to defect in thyroid hormone synthesis
- 2Hypothyroidism due to fibrous invasive thyroiditis
Get this concept via the API
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