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237517001: Congenital atrophy of thyroid (disorder)

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

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

\Disease\Disorder of foetus and/or newborn\Congenital disease\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)\Disorder of thyroid gland\Degeneration of thyroid (disorder)\Thyroid atrophy\Congenital atrophy of thyroid
\Disease\Disease of neck\Disorder of thyroid gland\Degeneration of thyroid (disorder)\Thyroid atrophy\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	Existential restriction modifier (core metadata concept)
Congenital atrophy of thyroid	Is a	Congenital anomaly of the thyroid gland	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital atrophy of thyroid	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital atrophy of thyroid	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital atrophy of thyroid	Finding site	Thyroid structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital atrophy of thyroid	Associated etiologic finding	Iodine deficiency	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital atrophy of thyroid	Associated morphology	Congenital deficiency	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital atrophy of thyroid	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital atrophy of thyroid	Is a	Thyroid atrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital atrophy of thyroid	Associated morphology	Congenital atrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital atrophy of thyroid	Associated morphology	Congenital atrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital atrophy of thyroid	Finding site	Thyroid structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital atrophy of thyroid	Is a	Congenital disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital atrophy of thyroid	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital atrophy of thyroid	Associated morphology	Atrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital atrophy of thyroid	Finding site	Thyroid structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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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
355960013	Congenital atrophy of thyroid	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character 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
5018721000241111	atrophie congénitale de la glande thyroïde	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5018721000241111	atrophie congénitale de la glande thyroïde	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module