Hypothyroidism diagnosis codes
Codelist metadata
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Coding system
- SNOMED CT
-
Coding system release
- unknown
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Organisation
- NHSD Primary Care Domain Refsets
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Codelist ID
- nhsd-primary-care-domain-refsets/thy_cod
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Version Tag
- 20200812
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Version ID
- 690c3189
Versions
About
Description
Taken from the THY_COD refset published by NHSD.
References
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 102871000119101 | Hypothyroidism due to thyroiditis |
| 10718002 | Juvenile myxedema |
| 10809101000119109 | Hypothyroidism in childbirth |
| 111308000 | Neurologic form of cretinism |
| 111566002 | Acquired hypothyroidism |
| 14779006 | Hypothyroidism following external radiotherapy |
| 17885001 | Iodotyrosine deiodination defect |
| 18621008 | Transient decreased production of T>4< |
| 190268003 | Congenital hypothyroidism |
| 190277005 | Irradiation hypothyroidism |
| 190279008 | Iodine hypothyroidism |
| 190282003 | Hypothyroidism resulting from para-aminosalicylic acid |
| 190283008 | Hypothyroidism resulting from phenylbutazone |
| 190284002 | Hypothyroidism resulting from resorcinol |
| 190304001 | Dyshormonogenic goiter |
| 190309006 | Thyroid atrophy |
| 21263006 | Myxedema coma |
| 215677009 | Congenital hypothyroidism with ectopic thyroid |
| 216693007 | Hypothyroid dwarfism |
| 217710005 | Congenital iodine deficiency syndrome |
| 22558005 | Iodide transport defect |
| 23536000 | Iodotyrosyl coupling defect |
| 237515009 | Congenital hypothyroidism without goiter |
| 237516005 | Congenital thyroid hypoplasia |
| 237517001 | Congenital atrophy of thyroid |
| 237518006 | Hypothyroid goiter, acquired |
| 237519003 | Autoimmune hypothyroidism |
| 237520009 | Hypothyroidism due to Hashimoto's thyroiditis |
| 237521008 | Hypothyroidism due to thyroid stimulating hormone receptor blocking antibody |
| 237523006 | Compensated hypothyroidism |
| 237525004 | Compensated euthyroidism |
| 237526003 | Euthyroid with thyroid antibodies |
| 237527007 | Postablative hypothyroidism |
| 237528002 | Post-infectious hypothyroidism |
| 237554005 | Familial dyshormonogenetic goiter |
| 237555006 | Hypothyroidism due to iodide trapping defect |
| 237556007 | Hypothyroidism due to iodide organification defect |
| 237559000 | Thyroid hormone resistance syndrome |
| 237560005 | Generalized thyroid hormone resistance |
| 237562002 | Iodine deficiency syndrome |
| 237565000 | Congenital iodine deficiency syndrome - mixed type |
| 237566004 | Congenital iodine deficiency syndrome - neurological type |
| 237567008 | Subclinical iodine deficiency hypothyroidism |
| 237695004 | Idiopathic thyroid stimulating hormone deficiency |
| 26692000 | Central hypothyroidism |
| 27059002 | Postoperative hypothyroidism |
| 276566003 | Transient neonatal hypothyroidism |
| 276630006 | Transient hypothyrotropinemia |
| 278503003 | Congenital hypothyroidism with diffuse goiter |
| 286910004 | Hypothyroidism - congenital and acquired |
| 2917005 | Transient hypothyroidism |
| 30229009 | Hypothyroidism due to infiltrative disease |
| 360348000 | Pituitary thyroid hormone resistance |
| 367631000119105 | Hypothyroidism caused by drug |
| 3716002 | Goiter |
| 37429009 | Hypothalamic hypothyroidism |
| 39444001 | Hypothyroidism due to fibrous invasive thyroiditis |
| 40539002 | Hypothyroidism following radioiodine therapy |
| 405629002 | Infant hypothyroidism |
| 405630007 | Infant hypothyroidism to 24 months of age |
| 40930008 | Hypothyroidism |
| 42277004 | Transient decreased production of T>3< |
| 42785009 | Hypothyroidism due to cystinosis |
| 428165003 | Hypothyroidism in pregnancy |
| 43153006 | Myxedema |
| 43507005 | Adult myxedema |
| 440092001 | Endemic congenital iodine deficiency syndrome of myxedematous type |
| 4641009 | Myxedema heart disease |
| 49830003 | Hypothyroidism caused by food stuff |
| 50375007 | Thyroid hormone responsiveness defect |
| 52724003 | Iodide oxidation defect |
| 54823002 | Subclinical hypothyroidism |
| 55838005 | Athyrotic hypothyroidism sequence |
| 56041007 | Hypothyroidism due to defect in thyroid hormone synthesis |
| 60733007 | Hypothyroidism due to amyloidosis |
| 63115005 | Hypothyroidism due to scleroderma |
| 63127008 | Thyroglobulin synthesis defect |
| 64491003 | Myxedematous form of cretinism |
| 698577000 | Infant hypothyroidism caused by maternal drug |
| 70225006 | Hypothyroidism caused by iodide excess |
| 70348004 | Pendred's syndrome |
| 715734006 | Congenital absence of half of thyroid |
| 716338001 | Muscular pseudohypertrophy and hypothyroidism syndrome |
| 717333002 | Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody |
| 717334008 | Idiopathic congenital hypothyroidism |
| 718183003 | Familial thyroid dyshormonogenesis |
| 718193005 | Peripheral resistance to thyroid hormone |
| 718194004 | Hypothyroidism due to mutation in transcription factor of pituitary development |
| 718690009 | Congenital hypothyroidism due to absence of thyroid gland |
| 722051004 | Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome |
| 722375007 | Bamforth Lazarus syndrome |
| 722938007 | Congenital central hypothyroidism |
| 722939004 | Congenital hypothyroidism due to iodine deficiency |
| 722940002 | Acquired central hypothyroidism |
| 725462002 | Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency |
| 74728003 | Hypopituitarism |
| 75065003 | Endemic cretinism |
| 763890006 | Short stature with delayed bone age due to thyroid hormone metabolism deficiency |
| 771510006 | X-linked central congenital hypothyroidism with late-onset testicular enlargement |
| 78574007 | Hypothyroidism due to sarcoidosis |
| 82598004 | Secondary hypothyroidism |
| 83664006 | Idiopathic atrophic hypothyroidism |
| 83986005 | Severe hypothyroidism |
| 84781002 | Sporadic cretinism |
| 88273006 | Iatrogenic hypothyroidism |
| 8868001 | Dyshormonogenetic goiter AND iodide leak |
| 89261000 | Isolated thyrotropin deficiency |
| 92978002 | Congenital absence of thyroid gland |
| 93359004 | Congenital malposition of the thyroid gland |
Codes not in the full codelist are in faint grey.