Application Version: 4.0.6.10
Content Version: 2024.07.12
Release Notes [PDF288KB]
User Guide [PDF6.08MB]
Code System Update Calendar
Contact Us
Subscribe
Related Links
- PHIN Vocabulary Services
- Quick Links / Mapping Tools
- External Standards Resources
- Message Guides
- Developer's Guide
- PHINVADS FHIR API
Downloads
- RCMT Quick Search
Code System Concept
Code System Concept Code | 17885001 |
Code System Concept Name | Iodotyrosine deiodination defect (disorder) |
Code System Preferred Concept Name | Iodotyrosine deiodination defect (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Superseded By Concept | |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 | 01/31/2002 |
SDO Date Created | 01/31/2002 |
SDO Date Revised | 01/31/2002 |
Description | |
Sequence |
Extended Properties
No extended properties.
Concept Alternate Designations
SDO Designation ID | Concept Designation Description | Status | Designation Type | PHIN Preferred Term Flag | Code Flag |
---|---|---|---|---|---|
30214011 | Iodotyrosine deiodination defect | Active | Synonym | false | false |
30215012 | Hypothyroidism due to iodotyrosine deiodinase defect | Active | Synonym | false | false |
30216013 | Genetic defect in thyroid hormonogenesis IV | Active | Synonym | false | false |
30217016 | Deiodinase deficiency | Active | Synonym | false | false |
30218014 | GDTH IV | Active | Synonym | false | false |
30219018 | Iodotyrosine deiodinase deficiency | Active | Synonym | false | false |
30220012 | Iodotyrosine dehalogenase deficiency | Active | Synonym | false | false |
478440011 | Hypothyroidism due to deiodase defect | Active | Synonym | false | false |
Parent Concepts
Parent Concepts
Parent/Child (Relationship Type)
Autosomal recessive hereditary disorder (disorder)
{85995004
, SNOMED-CT
}
Congenital hypothyroidism (disorder)
{190268003
, SNOMED-CT
}
Dyshormonogenic goiter (disorder)
{190304001
, SNOMED-CT
}
Enzymopathy (disorder)
{78548001
, SNOMED-CT
}
Hereditary disorder of endocrine system (disorder)
{363104002
, SNOMED-CT
}
Hypothyroidism (disorder)
{40930008
, SNOMED-CT
}
Inherited disorder of thyroid metabolism (disorder)
{36985004
, SNOMED-CT
}
Reproductive system hereditary disorder (disorder)
{363290007
, SNOMED-CT
}
|
Other Relationships
No other relationships present.
|
Child Concepts
No child concepts present.
|
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
- Content source: