191001007: Major histocompatibility complex class I deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Major histocompatibility complex class I deficiency
• \Disorder of immune function\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Major histocompatibility complex class I deficiency
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Severe combined immunodeficiency disease\Major histocompatibility complex class I deficiency
• \Disorder of immune function\Immunodeficiency disorder\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Major histocompatibility complex class I deficiency
• \Disorder of body system\Disorder of immune structure\Major histocompatibility complex class I deficiency
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Major histocompatibility complex class I deficiency
• \Congenital disease\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Major histocompatibility complex class I deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
293709012	Major histocompatibility complex class I deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
574649017	Major histocompatibility complex class I deficiency (disorder)	en	Fully specified name	Active	Initial character 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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