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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
293719018 Common variable immunodeficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
293719018 Common variable immunodeficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
574660014 Common variable immunodeficiency en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2756239016 Common variable immunodeficiency (disorder) en Fully specified name Active Only initial character 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 Existential restriction modifier (core metadata concept)
Common variable immunodeficiency Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Common variable immunodeficiency Is a Disorder of immune structure true Inferred relationship Existential restriction modifier (core metadata concept)
Common variable immunodeficiency Finding site Structure of immune system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Common variable agammaglobulinaemia Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Common variable immunodeficiency with autoantibodies to B- or T-cells (disorder) Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive common variable immunodeficiency due to CD81 deficiency (disorder) Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Common variable immunodeficiency due to transmembrane activator and calcium-modulator and cyclophilin ligand interactor deficiency (disorder) Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
X-linked common variable immunodeficiency due to SH3 domain containing kinase binding protein 1 deficiency (disorder) Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive common variable immunodeficiency due to membrane spanning 4-domains A1 mutation (disorder) Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive common variable immunodeficiency due to CD21 mutation Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive combined variable immunodeficiency due to B cell-activating factor receptor mutation (disorder) Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant combined variable immunodeficiency due to tumor necrosis factor-like weak inducer of apoptosis mutation (disorder) Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant combined variable immunodeficiency due to NFKB1 mutation Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant combined variable immunodeficiency due to interferon regulatory factor 2 binding protein 2 mutation (disorder) Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive combined variable immunodeficiency due to Rho guanine nucleotide exchange factor 1 mutation (disorder) Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant combined variable immunodeficiency due to SEC61A1 mutation Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive combined variable immunodeficiency due to PIK3CG mutation Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive common variable immunodeficiency due to POU class 2 homeobox associating factor 1 mutation (disorder) Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency (disorder) Is a True Common variable immunodeficiency Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

SAME AS association reference set (foundation metadata concept)

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