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191013002: Common variable immunodeficiency with autoantibodies to B- or T-cells (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
293722016 Common variable immunodeficiency with autoantibodies to B- or T-cells en Synonym Active Initial character case insensitive SNOMED CT core
574663011 Common variable immunodeficiency with autoantibodies to B- or T-cells (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Common variable immunodeficiency with autoantibodies to B- or T-cells Pathological process Abnormal immune process true Inferred relationship Some 2
Common variable immunodeficiency with autoantibodies to B- or T-cells Is a Disorder of immune structure true Inferred relationship Some
Common variable immunodeficiency with autoantibodies to B- or T-cells Has definitional manifestation Immune system finding false Inferred relationship Some
Common variable immunodeficiency with autoantibodies to B- or T-cells Is a Common variable agammaglobulinaemia true Inferred relationship Some
Common variable immunodeficiency with autoantibodies to B- or T-cells Is a Hereditary disorder of immune system true Inferred relationship Some
Common variable immunodeficiency with autoantibodies to B- or T-cells Occurrence Congenital true Inferred relationship Some 3
Common variable immunodeficiency with autoantibodies to B- or T-cells Finding site Structure of immune system true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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