52724003: Iodide oxidation defect (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation à propos d'une région de la tête et du cou\Finding of neck region\...

\Finding of thyroid gland\affection de la glande thyroïde (trouble)\...

\hypothyroïdie\Congenital hypothyroidism\anomalie d'oxydation des iodures

\Inherited disorder of thyroid metabolism\anomalie d'oxydation des iodures

\affection du cou\affection de la glande thyroïde (trouble)\...

\hypothyroïdie\Congenital hypothyroidism\anomalie d'oxydation des iodures

\Inherited disorder of thyroid metabolism\anomalie d'oxydation des iodures

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\anomalie d'oxydation des iodures
\Disease\Genetic disease\maladie héréditaire\Inborn error of metabolism\Inherited disorder of thyroid metabolism\anomalie d'oxydation des iodures
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\anomalie d'oxydation des iodures
\Disease\affection d'un système corporel\pathologie endocrinologique\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\anomalie d'oxydation des iodures
\Disease\affection d'un système corporel\pathologie endocrinologique\affection de la glande thyroïde (trouble)\hypothyroïdie\Congenital hypothyroidism\anomalie d'oxydation des iodures
\Disease\affection d'un système corporel\pathologie endocrinologique\affection de la glande thyroïde (trouble)\Inherited disorder of thyroid metabolism\anomalie d'oxydation des iodures
\Disease\affection du cou\affection de la glande thyroïde (trouble)\hypothyroïdie\Congenital hypothyroidism\anomalie d'oxydation des iodures
\Disease\affection du cou\affection de la glande thyroïde (trouble)\Inherited disorder of thyroid metabolism\anomalie d'oxydation des iodures
\Disease\trouble métabolique\Inborn error of metabolism\Inherited disorder of thyroid metabolism\anomalie d'oxydation des iodures
\Disease\Congenital disease\Congenital hypothyroidism\anomalie d'oxydation des iodures
\Disease\Congenital disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\anomalie d'oxydation des iodures

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
anomalie d'oxydation des iodures	survenue (attribut)	congénital	false	Inferred relationship	Some
anomalie d'oxydation des iodures	est un(e) (attribut)	hypothyroïdie	false	Inferred relationship	Some
anomalie d'oxydation des iodures	est un(e) (attribut)	Inherited disorder of thyroid metabolism	true	Inferred relationship	Some
anomalie d'oxydation des iodures	est un(e) (attribut)	Congenital hypothyroidism	true	Inferred relationship	Some
anomalie d'oxydation des iodures	survenue (attribut)	congénital	true	Inferred relationship	Some	1
anomalie d'oxydation des iodures	localisation d'une constatation (attribut)	structure de la thyroïde	true	Inferred relationship	Some	1
anomalie d'oxydation des iodures	localisation d'une constatation (attribut)	structure de la thyroïde	false	Inferred relationship	Some
anomalie d'oxydation des iodures	localisation d'une constatation (attribut)	Entire endocrine gonad (body structure)	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
313091000077119	anomalie d'oxydation des iodures	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
596541000077110	anomalie d'oxydation des iodures (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
790765011	Iodide oxidation defect (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
87732011	Iodide oxidation defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
87733018	Hypothyroidism due to iodide organification defect I	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
87734012	Iodide organification defect I	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
87735013	Thyroid hormone organification defect II A	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
87736014	GDTH IIA	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
87737017	Genetic defect in thyroid hormonogenesis II A	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core