Application Version: 4.0.6.10
Content Version: 2024.07.12
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Code System Concept
Code System Concept Code | 57185003 |
Code System Concept Name | Primary hypothyroidism (disorder) |
Code System Preferred Concept Name | Primary hypothyroidism (disorder) |
Concept Status | Published |
Concept Status Date | 09/01/2024 |
Code System Name | SNOMED-CT |
Concept Details
Code System Code | PH_SNOMED-CT |
Code System OID | 2.16.840.1.113883.6.96 |
HL7 Table 0396 Code | SCT |
Superseded By Concept | |
SDO Concept Status | Active |
SDO Concept Status Date | 07/31/2020 |
SDO Date Created | 01/31/2002 |
SDO Date Revised | 07/31/2020 |
Description | Disorder with characteristics of high serum thyroid-stimulating hormone (TSH) concentration and a low serum free thyroxine (T4) concentration. |
Sequence |
Extended Properties
No extended properties.
Concept Alternate Designations
SDO Designation ID | Concept Designation Description | Status | Designation Type | PHIN Preferred Term Flag | Code Flag |
---|---|---|---|---|---|
95113013 | Primary hypothyroidism | Active | Synonym | false | false |
Parent Concepts
Parent Concepts
Parent/Child (Relationship Type)
|
Other Relationships
No other relationships present.
|
Child Concepts
Primary hypothyroidism (disorder) {57185003 , SNOMED-CT }
Parent/Child (Relationship Type)
Autoimmune hypothyroidism (disorder)
{237519003
, SNOMED-CT
}
Familial thyroid dyshormonogenesis (disorder)
{718183003
, SNOMED-CT
}
Hypothyroidism due to defect in thyroid hormone synthesis (disorder)
{56041007
, SNOMED-CT
}
Hypothyroidism due to iodide trapping defect (disorder)
{237555006
, SNOMED-CT
}
Idiopathic congenital hypothyroidism (disorder)
{717334008
, SNOMED-CT
}
Iodide transport defect (disorder)
{22558005
, SNOMED-CT
}
Resistance to thyroid hormone due to mutation in thyroid hormone receptor alpha (disorder)
{1260240000
, SNOMED-CT
}
|
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
- Content source: