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715734006: congenitale afwezigheid van helft van schildklier (aandoening)


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
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
8687271000146116 congenitale afwezigheid van helft van schildklier nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8687281000146119 congenitale afwezigheid van helft van thyroïd nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8687291000146117 congenitale afwezigheid van helft van glandula thyroidea nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8687301000146118 congenitale afwezigheid van helft van schildklier (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3303560018 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. In symptomatic cases, clinical features and signs may include decreased activity and increased sleep, feeding difficulty, constipation and prolonged jaundice. Slow linear growth and developmental delay may also occur. Some familial cases have been reported suggesting genetic factors but to date none have been identified in humans. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital absence of half of thyroid (disorder) Is a Congenital absence of thyroid gland true Inferred relationship Some
Congenital absence of half of thyroid (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 1
Congenital absence of half of thyroid (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital absence of half of thyroid (disorder) Finding site Thyroid part true Inferred relationship Some 1
Congenital absence of half of thyroid (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital absence of half of thyroid (disorder) Associated morphology Absence (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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