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52724003: Iodide oxidation defect (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
790765011 Iodide oxidation defect (disorder) en Fully specified name Active Case insensitive SNOMED CT core
87732011 Iodide oxidation defect en Synonym Active Case insensitive SNOMED CT core
87733018 Hypothyroidism due to iodide organification defect I en Synonym Active Initial character case insensitive SNOMED CT core
87734012 Iodide organification defect I en Synonym Active Initial character case insensitive SNOMED CT core
87735013 Thyroid hormone organification defect II A en Synonym Active Initial character case insensitive SNOMED CT core
87736014 GDTH IIA en Synonym Active Case sensitive SNOMED CT core
87737017 Genetic defect in thyroid hormonogenesis II A en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Iodide oxidation defect Occurrence Congenital false Inferred relationship Some
Iodide oxidation defect Is a Hypothyroidism false Inferred relationship Some
Iodide oxidation defect Is a Inherited disorder of thyroid metabolism true Inferred relationship Some
Iodide oxidation defect Is a Congenital hypothyroidism true Inferred relationship Some
Iodide oxidation defect Occurrence Congenital true Inferred relationship Some 1
Iodide oxidation defect Finding site Thyroid structure true Inferred relationship Some 1
Iodide oxidation defect Finding site Thyroid structure false Inferred relationship Some
Iodide oxidation defect Finding site Entire endocrine gonad false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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