26692000: Central hypothyroidism (disorder)

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

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

\Disease\Disorder of body system\Disorder of endocrine system\Disorder of thyroid gland\Hypothyroidism (disorder)\Central hypothyroidism
\Disease\Disorder of neck (disorder)\Disorder of thyroid gland\Hypothyroidism (disorder)\Central hypothyroidism

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

44685019 Central hypothyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

757173017 Central hypothyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4005481000005114 central hypotyroidisme da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Central hypothyroidism	Is a	Hypothyroidism (disorder)	true	Inferred relationship	Some
Central hypothyroidism	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Some
Central hypothyroidism	Finding site	Thyroid structure	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hypothalamic hypothyroidism	Is a	True	Central hypothyroidism	Inferred relationship	Some
Congenital central hypothyroidism (disorder)	Is a	True	Central hypothyroidism	Inferred relationship	Some
Acquired central hypothyroidism (disorder)	Is a	True	Central hypothyroidism	Inferred relationship	Some
A rare genetic endocrine disease with characteristics of central hypothyroidism, testis enlargement in adolescence resulting in adult macroorchidism, delayed pubertal testosterone rise with a subsequent delayed pubertal growth spurt, small thyroid gland, and variable prolactin and growth hormone deficiency. Caused by mutation in the IGSF1 gene on chromosome Xq26.	Is a	True	Central hypothyroidism	Inferred relationship	Some

This concept is not in any reference sets