| Package | us.nlm.vsac |
| Type | ValueSet |
| Id | Id |
| FHIR Version | R4 |
| Source | http://fhir.org/packages/us.nlm.vsac/https://vsac.nlm.nih.gov/valueset/2.16.840.1.113762.1.4.1222.745/expansion |
| Url | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.745 |
| Version | 20240712 |
| Status | active |
| Date | 2024-07-12T01:03:21-04:00 |
| Name | Hypothyroidism |
| Title | Hypothyroidism |
| Experimental | False |
| Realm | us |
| Authority | hl7 |
| Purpose | (Clinical Focus: This set of values addresses terms representing Hypothyroidism.),(Data Element Scope: The intent of this set of values is to identify patients who have a/an documented diagnosis of hypothyroidism.),(Inclusion Criteria: Includes GROUP codes for Hypothyroidism.),(Exclusion Criteria: Terms not representative of observable encoded terms that may have values indicating Hypothyroidism.) |
No resources found
| CodeSystem | |
http://snomed.info/sct  | SNOMED CT (all versions) |
| http://hl7.org/fhir/sid/icd-10-cm | International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM) |
| http://snomed.info/sct | Nutrition Care Process Terminology module |
| http://snomed.info/sct | veri |
| http://hl7.org/fhir/sid/icd-10-cm | International Classification of Diseases, 10th Revision, Clinical Modification (ICD-10-CM) |
| http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.743 | Hypothyroidism |
| http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.744 | Hypothyroidism |
FHIR{
"resourceType" : "ValueSet",
"id" : "2.16.840.1.113762.1.4.1222.745",
"meta" : {
"versionId" : "11",
"lastUpdated" : "2024-09-12T22:33:45.000-04:00",
"profile" : [
"http://hl7.org/fhir/StructureDefinition/shareablevalueset",
"http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/computable-valueset-cqfm",
"http://hl7.org/fhir/us/cqfmeasures/StructureDefinition/publishable-valueset-cqfm"
]
},
"extension" : [
{
"url" : "http://hl7.org/fhir/StructureDefinition/valueset-author",
"valueContactDetail" : {
"name" : "MCC eCare Plan Author"
}
},
{
"url" : "http://hl7.org/fhir/StructureDefinition/valueset-keyWord",
"valueString" : "MCC_IG"
},
{
"url" : "http://hl7.org/fhir/StructureDefinition/resource-lastReviewDate",
"valueDate" : "2024-07-12"
},
{
"url" : "http://hl7.org/fhir/StructureDefinition/valueset-effectiveDate",
"valueDate" : "2024-07-12"
}
],
"url" : "http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.745",
"identifier" : [
{
"system" : "urn:ietf:rfc:3986",
"value" : "urn:oid:2.16.840.1.113762.1.4.1222.745"
}
],
"version" : "20240712",
"name" : "Hypothyroidism",
"title" : "Hypothyroidism",
"status" : "active",
"date" : "2024-07-12T01:03:21-04:00",
"publisher" : "HL7 Patient Care WG Steward",
"jurisdiction" : [
{
"coding" : [
{
"system" : "urn:iso:std:iso:3166",
"code" : "US"
}
]
}
],
"purpose" : "(Clinical Focus: This set of values addresses terms representing Hypothyroidism.),(Data Element Scope: The intent of this set of values is to identify patients who have a/an documented diagnosis of hypothyroidism.),(Inclusion Criteria: Includes GROUP codes for Hypothyroidism.),(Exclusion Criteria: Terms not representative of observable encoded terms that may have values indicating Hypothyroidism.)",
"compose" : {
"include" : [
{
"valueSet" : [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.744"
]
},
{
"valueSet" : [
"http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.743"
]
}
]
},
"expansion" : {
"identifier" : "urn:uuid:7b0214ea-2029-4bcc-94d2-14230a8c9547",
"timestamp" : "2024-12-10T08:33:29-05:00",
"total" : 140,
"contains" : [
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "102871000119101",
"display" : "Hypothyroidism due to thyroiditis (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "10718002",
"display" : "Juvenile myxedema (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "10753681000119101",
"display" : "Postpartum hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "10809101000119109",
"display" : "Hypothyroidism in childbirth (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "111566002",
"display" : "Acquired hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "111567006",
"display" : "Refetoff syndrome (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1137378008",
"display" : "Hypothyroidism due to and following radiotherapy (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1142106007",
"display" : "Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1156181008",
"display" : "Adrenocorticotropic hormone resistance syndrome (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1179381000",
"display" : "Acquired central hypothyroidism due to Sheehan syndrome (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1179382007",
"display" : "Acquired central hypothyroidism due to disorder of pituitary gland (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1179384008",
"display" : "Acquired central hypothyroidism caused by ionizing radiation (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1179385009",
"display" : "Acquired central hypothyroidism caused by drug (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1179392004",
"display" : "Acquired central hypothyroidism due to traumatic injury (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1179394003",
"display" : "Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1179395002",
"display" : "Consumptive hypothyroidism caused by type 3 iodothyronine deiodinase (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1179396001",
"display" : "Congenital hypothyroidism due to thyroid deiodinase mutation (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1179397005",
"display" : "Congenital hypothyroidism due to symporter mutation (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1179399008",
"display" : "Congenital hypothyroidism due to thyroglobulin mutation (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1179400001",
"display" : "Congenital hypothyroidism due to dual oxidase maturation factor 2 (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1179401002",
"display" : "Congenital hypothyroidism due to peripheral resistance to thyroid hormone (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1179404005",
"display" : "Congenital hypothyroidism due to congenital anomaly of thyroid gland (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1230272009",
"display" : "Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1259591007",
"display" : "Dementia due to acquired hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1260240000",
"display" : "Resistance to thyroid hormone due to mutation in thyroid hormone receptor alpha (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "1264402008",
"display" : "Hypothyroidism due to systemic sclerosis (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "14779006",
"display" : "Hypothyroidism following external radiotherapy (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "17885001",
"display" : "Iodotyrosine deiodination defect (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "18621008",
"display" : "Transient decreased production of T>4< (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "190268003",
"display" : "Congenital hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "190277005",
"display" : "Hypothyroidism caused by radiation (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "190279008",
"display" : "Iodine hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "190282003",
"display" : "Hypothyroidism resulting from para-aminosalicylic acid (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "190283008",
"display" : "Hypothyroidism resulting from phenylbutazone (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "190284002",
"display" : "Hypothyroidism caused by resorcinol (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "190304001",
"display" : "Dyshormonogenic goiter (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "206457007",
"display" : "Neonatal jaundice with congenital hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "216693007",
"display" : "Hypothyroid dwarfism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "22558005",
"display" : "Iodide transport defect (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "23536000",
"display" : "Iodotyrosyl coupling defect (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237515009",
"display" : "Congenital hypothyroidism without goiter (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237518006",
"display" : "Hypothyroid goiter, acquired (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237519003",
"display" : "Autoimmune hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237520009",
"display" : "Hypothyroidism due to Hashimoto's thyroiditis (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237521008",
"display" : "Hypothyroidism due to thyroid stimulating hormone receptor blocking antibody (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237526003",
"display" : "Euthyroid with thyroid antibodies (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237527007",
"display" : "Postablative hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237528002",
"display" : "Post-infectious hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237554005",
"display" : "Familial dyshormonogenetic goiter (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237555006",
"display" : "Hypothyroidism due to iodide trapping defect (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237556007",
"display" : "Hypothyroidism due to iodide organification defect (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237559000",
"display" : "Thyroid hormone resistance syndrome (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237560005",
"display" : "Generalized thyroid hormone resistance (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237565000",
"display" : "Congenital iodine deficiency syndrome of mixed type (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237567008",
"display" : "Subclinical iodine deficiency hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "237695004",
"display" : "Idiopathic thyroid stimulating hormone deficiency (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "26692000",
"display" : "Central hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "27059002",
"display" : "Postoperative hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "276566003",
"display" : "Transient neonatal hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "276630006",
"display" : "Transient hypothyrotropinemia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "278503003",
"display" : "Congenital hypothyroidism with diffuse goiter (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "2917005",
"display" : "Transient hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "30229009",
"display" : "Hypothyroidism due to infiltrative disease (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "360348000",
"display" : "Pituitary thyroid hormone resistance (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "360353005",
"display" : "Thyrotoxicosis due to pituitary thyroid hormone resistance (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "367631000119105",
"display" : "Hypothyroidism caused by drug (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "369091000119106",
"display" : "Hypothyroidism caused by amiodarone (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "37429009",
"display" : "Hypothalamic hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "39444001",
"display" : "Hypothyroidism due to fibrous invasive thyroiditis (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "40539002",
"display" : "Hypothyroidism following radioiodine therapy (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "405629002",
"display" : "Infant hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "405630007",
"display" : "Infant hypothyroidism to 24 months of age (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "40930008",
"display" : "Hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "42277004",
"display" : "Transient decreased production of T>3< (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "42785009",
"display" : "Hypothyroidism due to cystinosis (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "428165003",
"display" : "Hypothyroidism in pregnancy (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "43153006",
"display" : "Myxedema (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "43507005",
"display" : "Adult myxedema (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "440092001",
"display" : "Endemic congenital iodine deficiency syndrome of myxedematous type (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "45414006",
"display" : "Glucocorticoid deficiency with achalasia (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "4641009",
"display" : "Myxedema heart disease (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "49830003",
"display" : "Hypothyroidism caused by food stuff (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "50375007",
"display" : "Thyroid hormone responsiveness defect (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "52724003",
"display" : "Iodide oxidation defect (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "54823002",
"display" : "Subclinical hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "55838005",
"display" : "Athyrotic hypothyroidism sequence (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "56041007",
"display" : "Hypothyroidism due to defect in thyroid hormone synthesis (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "57185003",
"display" : "Primary hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "60733007",
"display" : "Hypothyroidism due to amyloidosis (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "63115005",
"display" : "Hypothyroidism due to scleroderma (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "63127008",
"display" : "Thyroglobulin synthesis defect (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "64491003",
"display" : "Myxedematous form of cretinism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "698577000",
"display" : "Infant hypothyroidism caused by maternal drug (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "699298009",
"display" : "Blepharophimosis, intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "70225006",
"display" : "Hypothyroidism caused by iodide excess (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "702327009",
"display" : "Monocarboxylate transporter 8 deficiency (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "716338001",
"display" : "Muscular pseudohypertrophy and hypothyroidism syndrome (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "717333002",
"display" : "Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "717334008",
"display" : "Idiopathic congenital hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "718183003",
"display" : "Familial thyroid dyshormonogenesis (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "718193005",
"display" : "Peripheral resistance to thyroid hormone (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "718194004",
"display" : "Hypothyroidism due to mutation in transcription factor of pituitary development (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "718690009",
"display" : "Congenital hypothyroidism due to absence of thyroid gland (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "722051004",
"display" : "Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "722375007",
"display" : "Bamforth Lazarus syndrome (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "722938007",
"display" : "Congenital central hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "722939004",
"display" : "Congenital hypothyroidism due to iodine deficiency (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "722940002",
"display" : "Acquired central hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "725462002",
"display" : "Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "763890006",
"display" : "Short stature with delayed bone age due to thyroid hormone metabolism deficiency (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "765326001",
"display" : "Familial glucocorticoid deficiency (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "770631009",
"display" : "Genetic transient congenital hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "771510006",
"display" : "X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "773987000",
"display" : "Transient neonatal hypothyroidism due to neonatal iodine exposure (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "783177006",
"display" : "Congenital hypothyroidism due to maternal intake of antithyroid drug (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "78574007",
"display" : "Hypothyroidism due to sarcoidosis (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "82598004",
"display" : "Secondary hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "83664006",
"display" : "Idiopathic atrophic hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "83986005",
"display" : "Severe hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "84781002",
"display" : "Sporadic cretinism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "88273006",
"display" : "Iatrogenic hypothyroidism (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "8868001",
"display" : "Dyshormonogenetic goiter AND iodide leak (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "89261000",
"display" : "Isolated thyrotropin deficiency (disorder)"
},
{
"system" : "http://snomed.info/sct",
"version" : "http://snomed.info/sct/731000124108/version/20240901",
"code" : "93359004",
"display" : "Congenital malposition of the thyroid gland (disorder)"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E00",
"display" : "Congenital iodine-deficiency syndrome"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E00.0",
"display" : "Congenital iodine-deficiency syndrome, neurological type"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E00.1",
"display" : "Congenital iodine-deficiency syndrome, myxedematous type"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E00.2",
"display" : "Congenital iodine-deficiency syndrome, mixed type"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E00.9",
"display" : "Congenital iodine-deficiency syndrome, unspecified"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E02",
"display" : "Subclinical iodine-deficiency hypothyroidism"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E03",
"display" : "Other hypothyroidism"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E03.0",
"display" : "Congenital hypothyroidism with diffuse goiter"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E03.1",
"display" : "Congenital hypothyroidism without goiter"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E03.2",
"display" : "Hypothyroidism due to medicaments and other exogenous substances"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E03.3",
"display" : "Postinfectious hypothyroidism"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E03.4",
"display" : "Atrophy of thyroid (acquired)"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E03.5",
"display" : "Myxedema coma"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E03.8",
"display" : "Other specified hypothyroidism"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E03.9",
"display" : "Hypothyroidism, unspecified"
},
{
"system" : "http://hl7.org/fhir/sid/icd-10-cm",
"version" : "2025",
"code" : "E89.0",
"display" : "Postprocedural hypothyroidism"
}
]
},
"text" : {
}
}
XIG built as of ??metadata-date??. Found ??metadata-resources?? resources in ??metadata-packages?? packages.