1179397005: congenitale hypothyreoïdie door mutatie van symportergen (aandoening)

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

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

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

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

Descriptions:

Id Description Lang Type Status Case? Module

4651007013 Congenital hypothyroidism due to symporter mutation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4651008015 Congenital hypothyroidism due to symporter mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

13308451000146116 congenitale hypothyreoïdie door mutatie van symportergen nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

13308461000146118 congenitale hypothyreoïdie door mutatie van symportergen (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

13308471000146112 congenitale hypothyroïdie door mutatie van symportergen 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
Congenital hypothyroidism due to symporter mutation (disorder)	Is a	Congenital hypothyroidism	true	Inferred relationship	Some
Congenital hypothyroidism due to symporter mutation (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Congenital hypothyroidism due to symporter mutation (disorder)	Finding site	Thyroid structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets