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191011000: Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
293720012 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions en Synonym Active Initial character case insensitive SNOMED CT core
574661013 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions (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 predominant abnormalities of B-cell numbers and functions Pathological process Abnormal immune process true Inferred relationship Some 2
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions Is a Disorder of immune structure true Inferred relationship Some
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions Has definitional manifestation Immune system finding false Inferred relationship Some
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions Is a Common variable agammaglobulinaemia true Inferred relationship Some
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions Is a Hereditary disorder of immune system true Inferred relationship Some
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions Occurrence Congenital true Inferred relationship Some 3
Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions 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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