1179399008: Congenital hypothyroidism due to thyroglobulin 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 thyroglobulin mutation (disorder)

\Disorder of neck (disorder)\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism\Congenital hypothyroidism due to thyroglobulin mutation (disorder)

\Disease\Disorder of body system\Disorder of endocrine system\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism\Congenital hypothyroidism due to thyroglobulin mutation (disorder)
\Disease\Disorder of neck (disorder)\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism\Congenital hypothyroidism due to thyroglobulin mutation (disorder)
\Disease\Congenital disease (disorder)\Congenital hypothyroidism\Congenital hypothyroidism due to thyroglobulin 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

4651011019 Congenital hypothyroidism due to thyroglobulin mutation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4651012014 Congenital hypothyroidism due to thyroglobulin mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

10705941000172111 hypothyroïdie congénitale due à une mutation de la thyréoglobuline fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

10705951000172113 hypothyroïdie congénitale due à une mutation de la thyroglobuline fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

7437431000172111 congenitale hypothyroïdie door mutatie van thyroglobuline-gen nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

7437441000172116 congenitale hypothyreoïdie door mutatie van thyreoglobuline-gen 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 thyroglobulin mutation (disorder)	Is a	Congenital hypothyroidism	true	Inferred relationship	Some
Congenital hypothyroidism due to thyroglobulin mutation (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Congenital hypothyroidism due to thyroglobulin mutation (disorder)	Finding site	Thyroid structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Description inactivation indicator reference set