FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.7.24 | FHIR Version n/a User: [n/a]

237517001: Congenital atrophy of thyroid (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\Degeneration of thyroid (disorder)\Thyroid atrophy\Congenital atrophy of thyroid

\Disorder of neck (disorder)\Disorder of thyroid gland\Degeneration of thyroid (disorder)\Thyroid atrophy\Congenital atrophy of thyroid

\Disease\Degenerative disorder\Degeneration of thyroid (disorder)\Thyroid atrophy\Congenital atrophy of thyroid
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of thyroid gland\Degeneration of thyroid (disorder)\Thyroid atrophy\Congenital atrophy of thyroid
\Disease\Disorder of neck (disorder)\Disorder of thyroid gland\Degeneration of thyroid (disorder)\Thyroid atrophy\Congenital atrophy of thyroid
\Disease\Congenital disease (disorder)\Congenital atrophy of thyroid

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital atrophy of thyroid	Is a	Congenital hypothyroidism without goitre	false	Inferred relationship	Some
Congenital atrophy of thyroid	Is a	Congenital anomaly of the thyroid gland	false	Inferred relationship	Some
Congenital atrophy of thyroid	Occurrence	Congenital	false	Inferred relationship	Some
Congenital atrophy of thyroid	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Some
Congenital atrophy of thyroid	Finding site	Thyroid structure	false	Inferred relationship	Some	1
Congenital atrophy of thyroid	Associated etiologic finding	Iodine deficiency	false	Inferred relationship	Some
Congenital atrophy of thyroid	Associated morphology	Congenital deficiency	false	Inferred relationship	Some
Congenital atrophy of thyroid	Associated morphology	Congenital malformation	false	Inferred relationship	Some
Congenital atrophy of thyroid	Is a	Thyroid atrophy	true	Inferred relationship	Some
Congenital atrophy of thyroid	Associated morphology	Congenital atrophy	false	Inferred relationship	Some	1
Congenital atrophy of thyroid	Associated morphology	Congenital atrophy	false	Inferred relationship	Some	1
Congenital atrophy of thyroid	Finding site	Thyroid structure	false	Inferred relationship	Some	1
Congenital atrophy of thyroid	Is a	Congenital disease (disorder)	true	Inferred relationship	Some
Congenital atrophy of thyroid	Occurrence	Congenital	true	Inferred relationship	Some	2
Congenital atrophy of thyroid	Associated morphology	Atrophy	true	Inferred relationship	Some	2
Congenital atrophy of thyroid	Finding site	Thyroid structure	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
355960013	Congenital atrophy of thyroid	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
626258016	Congenital atrophy of thyroid (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5592191000172117	atrophie congénitale de la glande thyroïde	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4698611000172119	aangeboren schildklieratrofie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4698621000172112	congenitale atrofie van schildklier	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)