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1230097004: atypisch lang-QT-intervalsyndroom type 8 (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5067142019 Atypical long QT syndrome type 8 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5067143012 Atypical Timothy syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5067144018 Atypical Timothy syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5067147013 Timothy syndrome atypical type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
13987181000146113 atypisch LQTS type 8 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13987191000146110 atypisch lang-QT-syndroom type 8 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13987201000146112 atypisch Timothy-syndroom nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13987211000146114 atypisch lang-QT-intervalsyndroom type 8 (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13987221000146116 atypisch lang-QT-intervalsyndroom type 8 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5067145017 A rare multiple congenital anomalies syndrome with cardiac involvement as a major feature with characteristics of QT prolongation, congenital heart defects, syndactyly, facial dysmorphism and neurodevelopmental features. The atypical form (ATS) causes multi-system health concerns but not necessarily with prolonged QT. The disease can be recognized by any CACNA1C change (excluding the G406R change) that causes multi-system health concerns. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5067146016 A rare multiple congenital anomalies syndrome with cardiac involvement as a major feature with characteristics of QT prolongation, congenital heart defects, syndactyly, facial dysmorphism and neurodevelopmental features. The atypical form (ATS) causes multi-system health concerns but not necessarily with prolonged QT. The disease can be recognised by any CACNA1C change (excluding the G406R change) that causes multi-system health concerns. 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
Atypical Timothy syndrome (disorder) Is a Timothy syndrome (disorder) true Inferred relationship Some
Atypical Timothy syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Atypical Timothy syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Atypical Timothy syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Atypical Timothy syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Atypical Timothy syndrome (disorder) Finding site Heart structure true Inferred relationship Some 2
Atypical Timothy syndrome (disorder) Finding site Cardiac conducting system structure true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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