1179397005: Congenital hypothyroidism due to symporter mutation (disorder)

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

\Finding of head and neck region\Finding of neck region\...

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

\Disorder of neck (disorder)\Disorder of thyroid gland\Hypothyroidism\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)
\Disease\Congenital disease (disorder)\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

10677721000172111 hypothyroïdie congénitale due à une mutation d'une protéine symport fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

10677731000172114 hypothyroïdie congénitale due à une mutation d'un symport fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

7421341000172118 congenitale hypothyroïdie door mutatie van symportergen nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

7421351000172116 congenitale hypothyreoïdie door mutatie van symportergen nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian 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

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Group

This concept is not in any reference sets