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191010004: Common variable immunodeficiency (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
293719018 Common variable immunodeficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2756239016 Common variable immunodeficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5255550015 CVID - common variable immunodeficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5255551016 Idiopathic immunoglobulin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5255552011 Primary hypogammaglobulinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5255553018 Primary antibody deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5255554012 Primary hypogammaglobulinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

18 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Common variable immunodeficiency Is a Primary immune deficiency disorder true Inferred relationship Some
Common variable immunodeficiency Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 1
Common variable immunodeficiency Is a Disorder of immune structure (disorder) true Inferred relationship Some
Common variable immunodeficiency Finding site Structure of immune system (body structure) true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Common variable agammaglobulinemia Is a True Common variable immunodeficiency Inferred relationship Some
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions Is a True Common variable immunodeficiency Inferred relationship Some
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) Is a True Common variable immunodeficiency Inferred relationship Some
Common variable immunodeficiency with autoantibodies to B- or T-cells Is a True Common variable immunodeficiency Inferred relationship Some
Autosomal recessive common variable immunodeficiency due to CD81 deficiency (disorder) Is a True Common variable immunodeficiency Inferred relationship Some
Common variable immunodeficiency due to transmembrane activator and calcium-modulator and cyclophilin ligand interactor deficiency (disorder) Is a True Common variable immunodeficiency Inferred relationship Some
X-linked common variable immunodeficiency due to SH3 domain containing kinase binding protein 1 deficiency (disorder) Is a True Common variable immunodeficiency Inferred relationship Some
Autosomal recessive common variable immunodeficiency due to membrane spanning 4-domains A1 mutation (disorder) Is a True Common variable immunodeficiency Inferred relationship Some
Autosomal recessive common variable immunodeficiency due to CD21 mutation Is a True Common variable immunodeficiency Inferred relationship Some
Autosomal recessive combined variable immunodeficiency due to B cell-activating factor receptor mutation (disorder) Is a True Common variable immunodeficiency Inferred relationship Some
Autosomal dominant combined variable immunodeficiency due to TWEAK mutation Is a True Common variable immunodeficiency Inferred relationship Some
Autosomal dominant combined variable immunodeficiency due to nuclear factor kappa B subunit 1 mutation (disorder) Is a True Common variable immunodeficiency Inferred relationship Some
Autosomal dominant combined variable immunodeficiency due to interferon regulatory factor 2 binding protein 2 mutation (disorder) Is a True Common variable immunodeficiency Inferred relationship Some
Autosomal recessive combined variable immunodeficiency due to ARHGEF1 mutation Is a True Common variable immunodeficiency Inferred relationship Some
Autosomal dominant combined variable immunodeficiency due to SEC61 translocon subunit alpha 1 mutation (disorder) Is a True Common variable immunodeficiency Inferred relationship Some
Autosomal recessive combined variable immunodeficiency due to PIK3CG mutation Is a True Common variable immunodeficiency Inferred relationship Some
Autosomal recessive common variable immunodeficiency due to POU class 2 homeobox associating factor 1 mutation (disorder) Is a True Common variable immunodeficiency Inferred relationship Some
Autosomal recessive common variable immunodeficiency due to RAC2 deficiency Is a True Common variable immunodeficiency Inferred relationship Some

This concept is not in any reference sets

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