403835002: X-linked hyper-immunoglobulin M syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\X-linked hyper-immunoglobulin M syndrome
• \Disorder of immune function\Immunodeficiency disorder\Congenital immunodeficiency disease\Congenital hypergammaglobulinemia\Hyperimmunoglobulin M syndrome\X-linked hyper-immunoglobulin M syndrome
• \Congenital disease\Congenital immunodeficiency disease\Congenital hypergammaglobulinemia\Hyperimmunoglobulin M syndrome\X-linked hyper-immunoglobulin M syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1771761011	X-linked hyper-IgM syndrome (disorder)	en	Fully specified name	Inactive	Entire term case sensitive	SNOMED CT core module
1782839018	X-linked hyper-IgM syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
1787887015	X-linked with hyper-IgM immunodeficiency	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
2970489019	X-linked hyper-immunoglobulin M syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
2970494019	X-linked hyper-immunoglobulin M syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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