191002000: Major histocompatibility complex class II 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 II deficiency
• \Disorder of immune function\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Major histocompatibility complex class II deficiency
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Severe combined immunodeficiency disease\Major histocompatibility complex class II deficiency
• \Disorder of immune function\Immunodeficiency disorder\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Major histocompatibility complex class II deficiency
• \Disorder of body system\Disorder of immune structure\Major histocompatibility complex class II deficiency
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Major histocompatibility complex class II deficiency
• \Congenital disease\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Major histocompatibility complex class II deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
293710019	Major histocompatibility complex class II deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
574650017	Major histocompatibility complex class II 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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