23536000: Iodotyrosyl coupling defect (disorder)

SNOMED CT Concept\constatation clinique\...

\Viscus structure finding (finding)\goitre\Dyshormonogenic goitre\anomalie du couplage des iodotyrosines

\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\Dyshormonogenic goitre\anomalie du couplage des iodotyrosines

\Inherited disorder of thyroid metabolism\anomalie du couplage des iodotyrosines

\goitre\Dyshormonogenic goitre\anomalie du couplage des iodotyrosines

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

\hypothyroïdie\Congenital hypothyroidism\Dyshormonogenic goitre\anomalie du couplage des iodotyrosines

\Inherited disorder of thyroid metabolism\anomalie du couplage des iodotyrosines

\goitre\Dyshormonogenic goitre\anomalie du couplage des iodotyrosines

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

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 du couplage des iodotyrosines	interprète (attribut)	Thyroid hormone measurement (procedure)	false	Inferred relationship	Some	3
anomalie du couplage des iodotyrosines	a pour interprétation (attribut)	au-dessus de l'étendue de référence	false	Inferred relationship	Some	3
anomalie du couplage des iodotyrosines	localisation d'une constatation (attribut)	Entire thyroid gland	true	Inferred relationship	Some	1
anomalie du couplage des iodotyrosines	morphologie associée (attribut)	Enlargement (morphologic abnormality)	true	Inferred relationship	Some	1
anomalie du couplage des iodotyrosines	survenue (attribut)	congénital	false	Inferred relationship	Some
anomalie du couplage des iodotyrosines	est un(e) (attribut)	hypothyroïdie	false	Inferred relationship	Some
anomalie du couplage des iodotyrosines	est un(e) (attribut)	Inherited disorder of thyroid metabolism	true	Inferred relationship	Some
anomalie du couplage des iodotyrosines	est un(e) (attribut)	Dyshormonogenic goitre	true	Inferred relationship	Some
anomalie du couplage des iodotyrosines	morphologie associée (attribut)	Hyperplasia (morphologic abnormality)	false	Inferred relationship	Some	1
anomalie du couplage des iodotyrosines	morphologie associée (attribut)	Hyperplasia (morphologic abnormality)	false	Inferred relationship	Some	1
anomalie du couplage des iodotyrosines	localisation d'une constatation (attribut)	structure de la thyroïde	false	Inferred relationship	Some	1
anomalie du couplage des iodotyrosines	morphologie associée (attribut)	Enlargement (morphologic abnormality)	false	Inferred relationship	Some	2
anomalie du couplage des iodotyrosines	localisation d'une constatation (attribut)	Entire thyroid gland	false	Inferred relationship	Some	2
anomalie du couplage des iodotyrosines	est un(e) (attribut)	Congenital hypothyroidism	false	Inferred relationship	Some
anomalie du couplage des iodotyrosines	survenue (attribut)	congénital	true	Inferred relationship	Some	1
anomalie du couplage des iodotyrosines	localisation d'une constatation (attribut)	Entire endocrine gonad (body structure)	false	Inferred relationship	Some
anomalie du couplage des iodotyrosines	localisation d'une constatation (attribut)	structure de la thyroïde	false	Inferred relationship	Some	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
1223110012	Hypothyroidism due to coupling defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
301371000077118	anomalie du couplage des iodotyrosines	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
39519010	Iodotyrosyl coupling defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
39520016	Congenital thyroid hormone coupling defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
39522012	Thyroid hormone coupling defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
39523019	Genetic defect in thyroid hormonogenesis III	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4590908018	GDTH III - genetic defect in thyroid hormonogenesis III	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
584121000077115	anomalie du couplage des iodotyrosines (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
753068012	Iodotyrosyl coupling defect (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core