1356782005: Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary disorder by system (disorder)\Hereditary disorder of immune system\Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency (disorder)
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency (disorder)
• \Disorder of immune function (disorder)\Hereditary disorder of immune system\Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency (disorder)
• \Disorder of immune function (disorder)\Immunodeficiency disorder\Primary immune deficiency disorder\Common variable immunodeficiency\Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency (disorder)
• \Disorder of body system\Disorder of immune structure\Common variable immunodeficiency\Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency (disorder)
• \Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of immune system\Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jan 2025. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5429343012	Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5429344018	Autosomal recessive common variable immunodeficiency due to RAC2 deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5429345017	Autosomal recessive common variable immunodeficiency due to RAC2 mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5429346016	Autosomal recessive CVID (common variable immunodeficiency) due to RAC2 mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5429347013	Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5429343012	Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5429344018	Autosomal recessive common variable immunodeficiency due to RAC2 deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5429345017	Autosomal recessive common variable immunodeficiency due to RAC2 mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5429346016	Autosomal recessive CVID (common variable immunodeficiency) due to RAC2 mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5429347013	Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

Back to Start