1351679006: Autosomal recessive agammaglobulinemia due to immunoglobulin alpha deficiency (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\...
• \Isolated agammaglobulinemia\Autosomal recessive agammaglobulinemia\Autosomal recessive agammaglobulinaemia due to immunoglobulin alpha deficiency
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Autosomal recessive agammaglobulinemia\Autosomal recessive agammaglobulinaemia due to immunoglobulin alpha deficiency
• \Disorder of immune function (disorder)\Immunodeficiency disorder\...
• \Primary immune deficiency disorder\Isolated agammaglobulinemia\Autosomal recessive agammaglobulinemia\Autosomal recessive agammaglobulinaemia due to immunoglobulin alpha deficiency
• \Congenital immunodeficiency disease\Congenital agammaglobulinemia\Isolated agammaglobulinemia\Autosomal recessive agammaglobulinemia\Autosomal recessive agammaglobulinaemia due to immunoglobulin alpha deficiency
• \Disorder of foetus and/or newborn\Congenital disease\Congenital immunodeficiency disease\Congenital agammaglobulinemia\Isolated agammaglobulinemia\Autosomal recessive agammaglobulinemia\Autosomal recessive agammaglobulinaemia due to immunoglobulin alpha 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
5414426011	Autosomal recessive agammaglobulinaemia due to immunoglobulin alpha deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5414427019	Autosomal recessive agammaglobulinaemia due to CD79A mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5414428012	Autosomal recessive agammaglobulinemia due to CD79A mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5414429016	Autosomal recessive agammaglobulinemia due to immunoglobulin alpha deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5414430014	Autosomal recessive agammaglobulinemia due to immunoglobulin alpha deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5414426011	Autosomal recessive agammaglobulinaemia due to immunoglobulin alpha deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5414427019	Autosomal recessive agammaglobulinaemia due to CD79A mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5414428012	Autosomal recessive agammaglobulinemia due to CD79A mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5414429016	Autosomal recessive agammaglobulinemia due to immunoglobulin alpha deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5414430014	Autosomal recessive agammaglobulinemia due to immunoglobulin alpha 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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