| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113762.1.4.1222.745 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.745 |
| version | 20210915 |
| status | active |
| publisher | HL7 Patient Care WG Steward |
| name | Hypothyroidism |
| title | Hypothyroidism |
| date | 2021-09-15T01:01:30-04:00 |
| experimental | false |
| description | This value set may undergo changes until the HL7 Multiple Chronic Care FHIR IG is formally published in 2024. |
| Usages | (none) |
This value set contains 133 concepts
| Code | System | Display |
| 102871000119101 | http://snomed.info/sct | Hypothyroidism due to thyroiditis (disorder) |
| 10718002 | http://snomed.info/sct | Juvenile myxedema (disorder) |
| 10809101000119109 | http://snomed.info/sct | Hypothyroidism in childbirth (disorder) |
| 111566002 | http://snomed.info/sct | Acquired hypothyroidism (disorder) |
| 111567006 | http://snomed.info/sct | Refetoff syndrome (disorder) |
| 1142106007 | http://snomed.info/sct | Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) |
| 1156181008 | http://snomed.info/sct | Adrenocorticotropic hormone resistance syndrome (disorder) |
| 1179381000 | http://snomed.info/sct | Acquired central hypothyroidism due to Sheehan syndrome (disorder) |
| 1179382007 | http://snomed.info/sct | Acquired central hypothyroidism due to disorder of pituitary gland (disorder) |
| 1179384008 | http://snomed.info/sct | Acquired central hypothyroidism caused by irradiation (disorder) |
| 1179385009 | http://snomed.info/sct | Acquired central hypothyroidism caused by drug (disorder) |
| 1179392004 | http://snomed.info/sct | Acquired central hypothyroidism due to traumatic injury (disorder) |
| 1179394003 | http://snomed.info/sct | Congenital hypothyroidism due to thyroid peroxidase mutation (disorder) |
| 1179395002 | http://snomed.info/sct | Consumptive hypothyroidism caused by type 3 iodothyronine deiodinase (disorder) |
| 1179396001 | http://snomed.info/sct | Congenital hypothyroidism due to thyroid deiodinase mutation (disorder) |
| 1179397005 | http://snomed.info/sct | Congenital hypothyroidism due to symporter mutation (disorder) |
| 1179399008 | http://snomed.info/sct | Congenital hypothyroidism due to thyroglobulin mutation (disorder) |
| 1179400001 | http://snomed.info/sct | Congenital hypothyroidism due to dual oxidase maturation factor 2 (disorder) |
| 1179401002 | http://snomed.info/sct | Congenital hypothyroidism due to peripheral resistance to thyroid hormone (disorder) |
| 1179404005 | http://snomed.info/sct | Congenital hypothyroidism due to congenital anomaly of thyroid gland (disorder) |
| 1230272009 | http://snomed.info/sct | Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation (disorder) |
| 17885001 | http://snomed.info/sct | Iodotyrosine deiodination defect (disorder) |
| 18621008 | http://snomed.info/sct | Transient decreased production of T>4< (disorder) |
| 190268003 | http://snomed.info/sct | Congenital hypothyroidism (disorder) |
| 190279008 | http://snomed.info/sct | Iodine hypothyroidism (disorder) |
| 190282003 | http://snomed.info/sct | Hypothyroidism resulting from para-aminosalicylic acid (disorder) |
| 190283008 | http://snomed.info/sct | Hypothyroidism resulting from phenylbutazone (disorder) |
| 190284002 | http://snomed.info/sct | Hypothyroidism caused by resorcinol (disorder) |
| 190304001 | http://snomed.info/sct | Dyshormonogenic goiter (disorder) |
| 206457007 | http://snomed.info/sct | Neonatal jaundice with congenital hypothyroidism (disorder) |
| 216693007 | http://snomed.info/sct | Hypothyroid dwarfism (disorder) |
| 22558005 | http://snomed.info/sct | Iodide transport defect (disorder) |
| 23536000 | http://snomed.info/sct | Iodotyrosyl coupling defect (disorder) |
| 237515009 | http://snomed.info/sct | Congenital hypothyroidism without goiter (disorder) |
| 237518006 | http://snomed.info/sct | Hypothyroid goiter, acquired (disorder) |
| 237519003 | http://snomed.info/sct | Autoimmune hypothyroidism (disorder) |
| 237520009 | http://snomed.info/sct | Hypothyroidism due to Hashimoto's thyroiditis (disorder) |
| 237521008 | http://snomed.info/sct | Hypothyroidism due to thyroid stimulating hormone receptor blocking antibody (disorder) |
| 237526003 | http://snomed.info/sct | Euthyroid with thyroid antibodies (disorder) |
| 237527007 | http://snomed.info/sct | Postablative hypothyroidism (disorder) |
| 237528002 | http://snomed.info/sct | Post-infectious hypothyroidism (disorder) |
| 237554005 | http://snomed.info/sct | Familial dyshormonogenetic goiter (disorder) |
| 237555006 | http://snomed.info/sct | Hypothyroidism due to iodide trapping defect (disorder) |
| 237556007 | http://snomed.info/sct | Hypothyroidism due to iodide organification defect (disorder) |
| 237559000 | http://snomed.info/sct | Thyroid hormone resistance syndrome (disorder) |
| 237560005 | http://snomed.info/sct | Generalized thyroid hormone resistance (disorder) |
| 237565000 | http://snomed.info/sct | Congenital iodine deficiency syndrome of mixed type (disorder) |
| 237567008 | http://snomed.info/sct | Subclinical iodine deficiency hypothyroidism (disorder) |
| 237695004 | http://snomed.info/sct | Idiopathic thyroid stimulating hormone deficiency (disorder) |
| 26692000 | http://snomed.info/sct | Central hypothyroidism (disorder) |
| 27059002 | http://snomed.info/sct | Postoperative hypothyroidism (disorder) |
| 276566003 | http://snomed.info/sct | Transient neonatal hypothyroidism (disorder) |
| 276630006 | http://snomed.info/sct | Transient hypothyrotropinemia (disorder) |
| 278503003 | http://snomed.info/sct | Congenital hypothyroidism with diffuse goiter (disorder) |
| 2917005 | http://snomed.info/sct | Transient hypothyroidism (disorder) |
| 30229009 | http://snomed.info/sct | Hypothyroidism due to infiltrative disease (disorder) |
| 360348000 | http://snomed.info/sct | Pituitary thyroid hormone resistance (disorder) |
| 360353005 | http://snomed.info/sct | Thyrotoxicosis due to pituitary thyroid hormone resistance (disorder) |
| 367631000119105 | http://snomed.info/sct | Hypothyroidism caused by drug (disorder) |
| 369091000119106 | http://snomed.info/sct | Hypothyroidism caused by amiodarone (disorder) |
| 37429009 | http://snomed.info/sct | Hypothalamic hypothyroidism (disorder) |
| 39444001 | http://snomed.info/sct | Hypothyroidism due to fibrous invasive thyroiditis (disorder) |
| 40539002 | http://snomed.info/sct | Hypothyroidism following radioiodine therapy (disorder) |
| 405629002 | http://snomed.info/sct | Infant hypothyroidism (disorder) |
| 405630007 | http://snomed.info/sct | Infant hypothyroidism to 24 months of age (disorder) |
| 40930008 | http://snomed.info/sct | Hypothyroidism (disorder) |
| 42277004 | http://snomed.info/sct | Transient decreased production of T>3< (disorder) |
| 42785009 | http://snomed.info/sct | Hypothyroidism due to cystinosis (disorder) |
| 428165003 | http://snomed.info/sct | Hypothyroidism in pregnancy (disorder) |
| 43153006 | http://snomed.info/sct | Myxedema (disorder) |
| 43507005 | http://snomed.info/sct | Adult myxedema (disorder) |
| 440092001 | http://snomed.info/sct | Endemic congenital iodine deficiency syndrome of myxedematous type (disorder) |
| 45414006 | http://snomed.info/sct | Glucocorticoid deficiency with achalasia (disorder) |
| 4641009 | http://snomed.info/sct | Myxedema heart disease (disorder) |
| 49830003 | http://snomed.info/sct | Hypothyroidism caused by food stuff (disorder) |
| 50375007 | http://snomed.info/sct | Thyroid hormone responsiveness defect (disorder) |
| 52724003 | http://snomed.info/sct | Iodide oxidation defect (disorder) |
| 54823002 | http://snomed.info/sct | Subclinical hypothyroidism (disorder) |
| 55838005 | http://snomed.info/sct | Athyrotic hypothyroidism sequence (disorder) |
| 56041007 | http://snomed.info/sct | Hypothyroidism due to defect in thyroid hormone synthesis (disorder) |
| 57185003 | http://snomed.info/sct | Primary hypothyroidism (disorder) |
| 60733007 | http://snomed.info/sct | Hypothyroidism due to amyloidosis (disorder) |
| 63115005 | http://snomed.info/sct | Hypothyroidism due to scleroderma (disorder) |
| 63127008 | http://snomed.info/sct | Thyroglobulin synthesis defect (disorder) |
| 64491003 | http://snomed.info/sct | Myxedematous form of cretinism (disorder) |
| 698577000 | http://snomed.info/sct | Infant hypothyroidism caused by maternal drug (disorder) |
| 699298009 | http://snomed.info/sct | Blepharophimosis, intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type (disorder) |
| 70225006 | http://snomed.info/sct | Hypothyroidism caused by iodide excess (disorder) |
| 702327009 | http://snomed.info/sct | Monocarboxylate transporter 8 deficiency (disorder) |
| 716338001 | http://snomed.info/sct | Muscular pseudohypertrophy and hypothyroidism syndrome (disorder) |
| 717333002 | http://snomed.info/sct | Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody (disorder) |
| 717334008 | http://snomed.info/sct | Idiopathic congenital hypothyroidism (disorder) |
| 718183003 | http://snomed.info/sct | Familial thyroid dyshormonogenesis (disorder) |
| 718193005 | http://snomed.info/sct | Peripheral resistance to thyroid hormone (disorder) |
| 718194004 | http://snomed.info/sct | Hypothyroidism due to mutation in transcription factor of pituitary development (disorder) |
| 718690009 | http://snomed.info/sct | Congenital hypothyroidism due to absence of thyroid gland (disorder) |
| 722051004 | http://snomed.info/sct | Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome (disorder) |
| 722375007 | http://snomed.info/sct | Bamforth Lazarus syndrome (disorder) |
| 722938007 | http://snomed.info/sct | Congenital central hypothyroidism (disorder) |
| 722939004 | http://snomed.info/sct | Congenital hypothyroidism due to iodine deficiency (disorder) |
| 722940002 | http://snomed.info/sct | Acquired central hypothyroidism (disorder) |
| 725462002 | http://snomed.info/sct | Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder) |
| 763890006 | http://snomed.info/sct | Short stature with delayed bone age due to thyroid hormone metabolism deficiency (disorder) |
| 765326001 | http://snomed.info/sct | Familial glucocorticoid deficiency (disorder) |
| 770631009 | http://snomed.info/sct | Genetic transient congenital hypothyroidism (disorder) |
| 771510006 | http://snomed.info/sct | X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) |
| 773987000 | http://snomed.info/sct | Transient neonatal hypothyroidism due to neonatal iodine exposure (disorder) |
| 783177006 | http://snomed.info/sct | Congenital hypothyroidism due to maternal intake of antithyroid drug (disorder) |
| 78574007 | http://snomed.info/sct | Hypothyroidism due to sarcoidosis (disorder) |
| 82598004 | http://snomed.info/sct | Secondary hypothyroidism (disorder) |
| 83664006 | http://snomed.info/sct | Idiopathic atrophic hypothyroidism (disorder) |
| 83986005 | http://snomed.info/sct | Severe hypothyroidism (disorder) |
| 84781002 | http://snomed.info/sct | Sporadic cretinism (disorder) |
| 88273006 | http://snomed.info/sct | Iatrogenic hypothyroidism (disorder) |
| 8868001 | http://snomed.info/sct | Dyshormonogenetic goiter AND iodide leak (disorder) |
| 89261000 | http://snomed.info/sct | Isolated thyrotropin deficiency (disorder) |
| 93359004 | http://snomed.info/sct | Congenital malposition of the thyroid gland (disorder) |
| E00 | http://hl7.org/fhir/sid/icd-10-cm | Congenital iodine-deficiency syndrome |
| E00.0 | http://hl7.org/fhir/sid/icd-10-cm | Congenital iodine-deficiency syndrome, neurological type |
| E00.1 | http://hl7.org/fhir/sid/icd-10-cm | Congenital iodine-deficiency syndrome, myxedematous type |
| E00.2 | http://hl7.org/fhir/sid/icd-10-cm | Congenital iodine-deficiency syndrome, mixed type |
| E00.9 | http://hl7.org/fhir/sid/icd-10-cm | Congenital iodine-deficiency syndrome, unspecified |
| E02 | http://hl7.org/fhir/sid/icd-10-cm | Subclinical iodine-deficiency hypothyroidism |
| E03 | http://hl7.org/fhir/sid/icd-10-cm | Other hypothyroidism |
| E03.0 | http://hl7.org/fhir/sid/icd-10-cm | Congenital hypothyroidism with diffuse goiter |
| E03.1 | http://hl7.org/fhir/sid/icd-10-cm | Congenital hypothyroidism without goiter |
| E03.2 | http://hl7.org/fhir/sid/icd-10-cm | Hypothyroidism due to medicaments and other exogenous substances |
| E03.3 | http://hl7.org/fhir/sid/icd-10-cm | Postinfectious hypothyroidism |
| E03.4 | http://hl7.org/fhir/sid/icd-10-cm | Atrophy of thyroid (acquired) |
| E03.5 | http://hl7.org/fhir/sid/icd-10-cm | Myxedema coma |
| E03.8 | http://hl7.org/fhir/sid/icd-10-cm | Other specified hypothyroidism |
| E03.9 | http://hl7.org/fhir/sid/icd-10-cm | Hypothyroidism, unspecified |
| E89.0 | http://hl7.org/fhir/sid/icd-10-cm | Postprocedural hypothyroidism |
Produced 08 Sep 2023