722938007: Congenital central hypothyroidism (disorder)

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

\Finding of neck region\Finding of thyroid gland\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism (disorder)\Congenital central hypothyroidism (disorder)
\Finding of neck region\Finding of thyroid gland\Disorder of thyroid gland\Hypothyroidism\Central hypothyroidism\Congenital central hypothyroidism (disorder)
\Finding of neck region\Disease of neck\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism (disorder)\Congenital central hypothyroidism (disorder)
\Finding of neck region\Disease of neck\Disorder of thyroid gland\Hypothyroidism\Central hypothyroidism\Congenital central hypothyroidism (disorder)

\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital hypothyroidism (disorder)\Congenital central hypothyroidism (disorder)
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism (disorder)\Congenital central hypothyroidism (disorder)
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disorder of thyroid gland\Hypothyroidism\Central hypothyroidism\Congenital central hypothyroidism (disorder)
\Disease\Disease of neck\Disorder of thyroid gland\Hypothyroidism\Congenital hypothyroidism (disorder)\Congenital central hypothyroidism (disorder)
\Disease\Disease of neck\Disorder of thyroid gland\Hypothyroidism\Central hypothyroidism\Congenital central hypothyroidism (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3333987011 Congenital central hypothyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3333988018 Congenital central hypothyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3333987011 Congenital central hypothyroidism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3333987011 Congenital central hypothyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3333988018 Congenital central hypothyroidism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3333988018 Congenital central hypothyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

874361000172114 hypothyroïdie congénitale centrale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

874361000172114 hypothyroïdie congénitale centrale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital central hypothyroidism (disorder)	Is a	Central hypothyroidism	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital central hypothyroidism (disorder)	Is a	Congenital hypothyroidism (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital central hypothyroidism (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital central hypothyroidism (disorder)	Finding site	Thyroid structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital central hypothyroidism (disorder)	Finding site	Thyroid structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Resistance to thyrotropin-releasing hormone (TRH) syndrome is a type of central congenital hypothyroidism characterised by low levels of thyroid hormones due to insufficient release of thyroid-stimulating hormone (TSH) caused by pituitary resistance to TRH. It may or may not be observed from birth.	Is a	True	Congenital central hypothyroidism (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets