1142106007: passagère congenitale hypothyreoïdie door mutatie van 'dual oxidase 2'-gen (aandoening)

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

\Finding of neck region\Finding of thyroid gland\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism\Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)
\Finding of neck region\Finding of thyroid gland\Disorder of thyroid gland\Hypothyroidism\Transient hypothyroidism\Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)
\Finding of neck region\Disorder of neck (disorder)\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism\Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)
\Finding of neck region\Disorder of neck (disorder)\Disorder of thyroid gland\Hypothyroidism\Transient hypothyroidism\Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)

\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital hypothyroidism\Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism\Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of thyroid gland\Hypothyroidism\Transient hypothyroidism\Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)
\Disease\Disorder of neck (disorder)\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism\Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)
\Disease\Disorder of neck (disorder)\Disorder of thyroid gland\Hypothyroidism\Transient hypothyroidism\Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)
\Disease\Acute disease\Transient hypothyroidism\Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4536636017 Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4536637014 Transient congenital hypothyroidism due to dual oxidase 2 mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

12966481000146111 voorbijgaande congenitale hypothyroïdie door mutatie van DUOX-2 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

12988101000146110 passagère congenitale hypothyreoïdie door mutatie van 'dual oxidase 2'-gen (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

12988111000146112 passagère congenitale hypothyreoïdie door mutatie van 'dual oxidase 2'-gen nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)	Is a	Congenital hypothyroidism	true	Inferred relationship	Some
Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)	Is a	Transient hypothyroidism	true	Inferred relationship	Some
Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)	Finding site	Thyroid structure	true	Inferred relationship	Some	1
Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)	Due to	Chromosomal disorder (disorder)	true	Inferred relationship	Some	2
Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)	Clinical course	Transitory	true	Inferred relationship	Some	3

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Description inactivation indicator reference set