1179394003: Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of neck region\Finding of thyroid gland\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism (disorder)\Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)
\Finding of neck region\Disease of neck\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism (disorder)\Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)

\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital hypothyroidism (disorder)\Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism (disorder)\Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)
\Disease\Disease of neck\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism (disorder)\Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)	Is a	Congenital hypothyroidism (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)	Finding site	Thyroid structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

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
4651001014	Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4651002019	Congenital hypothyroidism due to thyroid peroxidase mutation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4651001014	Congenital hypothyroidism due to thyroid peroxidase mutation (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4651002019	Congenital hypothyroidism due to thyroid peroxidase mutation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5858171000241119	hypothyroïdie congénitale due à une mutation de la thyroperoxydase	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5858181000241117	hypothyroïdie congénitale due à une mutation de la peroxydase thyroïdienne	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5858191000241115	hypothyroïdie congénitale due à une mutation de la TPO (thyroperoxydase)	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5858171000241119	hypothyroïdie congénitale due à une mutation de la thyroperoxydase	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5858181000241117	hypothyroïdie congénitale due à une mutation de la peroxydase thyroïdienne	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5858191000241115	hypothyroïdie congénitale due à une mutation de la TPO (thyroperoxydase)	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module