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58034007: Congenital hypergammaglobulinemia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
198804014 Congenital hypergammaglobulinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
498053010 Congenital hypergammaglobulinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
796722017 Congenital hypergammaglobulinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypergammaglobulinemia Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 2
Congenital hypergammaglobulinemia est un(e) (attribut) Congenital immunodeficiency disease true Inferred relationship Some
Congenital hypergammaglobulinemia est défini par la manifestation de (attribut) Immune system finding false Inferred relationship Some
Congenital hypergammaglobulinemia survenue (attribut) congénital true Inferred relationship Some 1
Congenital hypergammaglobulinemia localisation d'une constatation (attribut) structure du système immunitaire false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Hyperimmunoglobulin E syndrome est un(e) (attribut) False Congenital hypergammaglobulinemia Inferred relationship Some
Hyperimmunoglobulin M syndrome est un(e) (attribut) True Congenital hypergammaglobulinemia Inferred relationship Some
Hyperimmunoglobulin E syndrome est un(e) (attribut) True Congenital hypergammaglobulinemia Inferred relationship Some

This concept is not in any reference sets

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