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52724003: Iodide oxidation defect (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of head and neck region\Finding of neck region\...

\Finding of thyroid gland\Disorder of thyroid gland\...

\Hypothyroidism\Congenital hypothyroidism\Iodide oxidation defect

\Inherited disorder of thyroid metabolism\Iodide oxidation defect

\Disorder of neck\Disorder of thyroid gland\...

\Hypothyroidism\Congenital hypothyroidism\Iodide oxidation defect

\Inherited disorder of thyroid metabolism\Iodide oxidation defect

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Iodide oxidation defect
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Iodide oxidation defect
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Iodide oxidation defect
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Inherited disorder of thyroid metabolism\Iodide oxidation defect
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism\Iodide oxidation defect
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Iodide oxidation defect
\Disease\Disorder of neck\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism\Iodide oxidation defect
\Disease\Disorder of neck\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Iodide oxidation defect
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Iodide oxidation defect
\Disease\Congenital disease\Congenital hypothyroidism\Iodide oxidation defect
\Disease\Congenital disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Iodide oxidation defect

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

87732011 Iodide oxidation defect en Synonym Active Entire term case insensitive SNOMED CT core module

87733018 Hypothyroidism due to iodide organification defect I en Synonym Active Only initial character case insensitive SNOMED CT core module

87734012 Iodide organification defect I en Synonym Active Only initial character case insensitive SNOMED CT core module

87735013 Thyroid hormone organification defect II A en Synonym Active Only initial character case insensitive SNOMED CT core module

87736014 GDTH IIA en Synonym Active Entire term case sensitive SNOMED CT core module

87737017 Genetic defect in thyroid hormonogenesis II A en Synonym Active Only initial character case insensitive SNOMED CT core module

790765011 Iodide oxidation defect (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

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