1351570003: Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant hyperimmunoglobulin M syndrome due to AID deficiency
• \Disorder of immune function (disorder)\Immunodeficiency disorder\Primary immune deficiency disorder\...
• \Combined immunodeficiency disease\Hyperimmunoglobulin M syndrome without susceptibility to opportunistic infection (disorder)\Autosomal dominant hyperimmunoglobulin M syndrome due to AID deficiency
• \Hyperimmunoglobulin M syndrome\Hyperimmunoglobulin M syndrome without susceptibility to opportunistic infection (disorder)\Autosomal dominant hyperimmunoglobulin M syndrome due to AID deficiency

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Nov 2024. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5407825015	Autosomal dominant hyper IgM syndrome due to AICDA	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5407826019	Autosomal dominant hyperimmunoglobulin M syndrome due to AID deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5407827011	Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5407828018	Autosomal dominant hyper-IgM syndrome type 2	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5407829014	Autosomal dominant hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5407831017	Autosomal dominant activation-induced cytidine deaminase deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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