403836001: Autosomal recessive hyperimmunoglobulin M syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Autosomal recessive hyper-IgM syndrome
• \Disorder of immune function\Immunodeficiency disorder\Congenital immunodeficiency disease\Congenital hypergammaglobulinaemia\Hyper IgM syndrome\Autosomal recessive hyper-IgM syndrome
• \Congenital disease\Congenital immunodeficiency disease\Congenital hypergammaglobulinaemia\Hyper IgM syndrome\Autosomal recessive hyper-IgM syndrome

Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1782840016	Autosomal recessive hyper-IgM syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2968614012	Autosomal recessive hyper- immunoglobulin M syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3424904019	Autosomal recessive hyperimmunoglobulin M syndrome (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3424905018	Autosomal recessive hyperimmunoglobulin M syndrome	en	Synonym	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

Back to Start