49555001: Severe combined immunodeficiency due to absent T cell receptor (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\SCID due to absent T cell receptor
• \Disorder of immune function\Hereditary disorder of immune system\Severe combined immunodeficiency disease\SCID due to absent T cell receptor
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Severe combined immunodeficiency disease\SCID due to absent T cell receptor
• \Disorder of immune function\Immunodeficiency disorder\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\SCID due to absent T cell receptor
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\SCID due to absent T cell receptor
• \Congenital disease\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\SCID due to absent T cell receptor

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2620887012	Severe combined immunodeficiency (SCID) due to absent T cell receptor	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2913409018	Severe combined immunodeficiency due to absent T cell receptor	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2913672016	Severe combined immunodeficiency due to absent T cell receptor (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
82545018	SCID due to absent T cell receptor	en	Synonym	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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