234570002: Severe combined immunodeficiency with maternofetal engraftment (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency with maternofetal engraftment
• \Disorder of immune function\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency with maternofetal engraftment
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency with maternofetal engraftment
• \Disorder of immune function\Immunodeficiency disorder\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency with maternofetal engraftment
• \Disorder of body system\Disorder of immune structure\Severe combined immunodeficiency with maternofetal engraftment
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency with maternofetal engraftment
• \Congenital disease\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency with maternofetal engraftment

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3013782018	Severe combined immunodeficiency with maternofoetal engraftment	en	Synonym	Active	Case insensitive	SNOMED CT core
351460011	Severe combined immunodeficiency with maternofetal engraftment	en	Synonym	Active	Case insensitive	SNOMED CT core
622908016	Severe combined immunodeficiency with maternofetal engraftment (disorder)	en	Fully specified name	Active	Case insensitive	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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