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715734006: Congenital absence of half of thyroid (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5401063016 Thyroid hemiagenesis is a form of thyroid dysgenesis characterized by an absence of half of the thyroid gland that is usually asymptomatic but may result in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401064010 Thyroid hemiagenesis is a form of thyroid dysgenesis characterised by an absence of half of the thyroid gland that is usually asymptomatic but may result in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3303556016 Congenital absence of half of thyroid (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303557013 Congenital absence of half of thyroid en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303558015 Congenital hemiagenesis of thyroid en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303559011 Thyroid hemiagenesis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5904971000241110 absence congénitale de la moitié de la thyroïde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5904981000241112 absence congénitale de la moitié de la glande thyroïde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3419511001000110 Schilddrüsenhemiagenesie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Thyroid hemiagenesis is a form of thyroid dysgenesis characterized by an absence of half of the thyroid gland that is usually asymptomatic but may result in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. Is a Congenital absence of thyroid gland true Inferred relationship Some
Thyroid hemiagenesis is a form of thyroid dysgenesis characterized by an absence of half of the thyroid gland that is usually asymptomatic but may result in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. Associated morphology Congenital absence false Inferred relationship Some 1
Thyroid hemiagenesis is a form of thyroid dysgenesis characterized by an absence of half of the thyroid gland that is usually asymptomatic but may result in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. Occurrence Congenital true Inferred relationship Some 1
Thyroid hemiagenesis is a form of thyroid dysgenesis characterized by an absence of half of the thyroid gland that is usually asymptomatic but may result in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. Finding site Thyroid part true Inferred relationship Some 1
Thyroid hemiagenesis is a form of thyroid dysgenesis characterized by an absence of half of the thyroid gland that is usually asymptomatic but may result in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Thyroid hemiagenesis is a form of thyroid dysgenesis characterized by an absence of half of the thyroid gland that is usually asymptomatic but may result in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. Associated morphology Absence (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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