460495004: Long QT syndrome with genetic marker (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2922800017 Long QT syndrome with genetic marker (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2922801018 Long QT syndrome with genetic marker en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2922800017 Long QT syndrome with genetic marker (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2922801018 Long QT syndrome with genetic marker en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Long QT syndrome with genetic marker	Is a	Familial long QT syndrome	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Long QT syndrome with genetic marker	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Long QT syndrome with genetic marker	Finding site	Cardiac conducting system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Long QT syndrome with genetic marker	Finding site	Heart structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Romano-Ward syndrome (disorder)	Is a	False	Long QT syndrome with genetic marker	Inferred relationship	Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder)	Is a	False	Long QT syndrome with genetic marker	Inferred relationship	Existential restriction modifier (core metadata concept)
Andersen Tawil syndrome	Is a	False	Long QT syndrome with genetic marker	Inferred relationship	Existential restriction modifier (core metadata concept)
Timothy syndrome type 1	Is a	False	Long QT syndrome with genetic marker	Inferred relationship	Existential restriction modifier (core metadata concept)
Timothy syndrome type 2 (disorder)	Is a	False	Long QT syndrome with genetic marker	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

POSSIBLY EQUIVALENT TO association reference set