1351576009: Autosomal recessive hyperimmunoglobulin M syndrome due to mutator S homolog 6 deficiency (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary cancer-predisposing syndrome\Constitutional mismatch repair deficiency syndrome (disorder)\Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\...
• \Constitutional mismatch repair deficiency syndrome (disorder)\Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency
• \Autosomal recessive hyperimmunoglobulin M syndrome (disorder)\Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency
• \Disorder of immune function (disorder)\Immunodeficiency disorder\Primary immune deficiency disorder\...
• \Constitutional mismatch repair deficiency syndrome (disorder)\Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency
• \Hyperimmunoglobulin M syndrome\Autosomal recessive hyperimmunoglobulin M syndrome (disorder)\Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 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
5407858012	Autosomal recessive hyperimmunoglobulin M syndrome due to MSH6 deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5407859016	Hyper IgM syndrome due to MSH6	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5407860014	Autosomal recessive hyperimmunoglobulin M syndrome due to mutS homolog 6 deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5407861013	Autosomal recessive hyperimmunoglobulin M syndrome due to mutator S homolog 6 deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5407862018	Autosomal recessive hyperimmunoglobulin M syndrome due to mutator S homolog 6 deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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