58034007: Congenital hypergammaglobulinemia (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Disorder of immune function (disorder)\Immunodeficiency disorder\Congenital immunodeficiency disease\Congenital hypergammaglobulinaemia

\Disorder of foetus and/or newborn\Congenital disease\Congenital immunodeficiency disease\Congenital hypergammaglobulinaemia

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

198804014 Congenital hypergammaglobulinemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

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 Only initial character 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 Only initial character 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

4580211000241118 hypergammaglobulinémie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4580211000241118 hypergammaglobulinémie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital hypergammaglobulinaemia	Is a	Congenital immunodeficiency disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hypergammaglobulinaemia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypergammaglobulinaemia	Finding site	Structure of immune system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hypergammaglobulinaemia	Has definitional manifestation	Immune system finding	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hypergammaglobulinaemia	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hyperimmunoglobulin E syndrome	Is a	False	Congenital hypergammaglobulinaemia	Inferred relationship	Existential restriction modifier (core metadata concept)
Hyperimmunoglobulin M syndrome (disorder)	Is a	False	Congenital hypergammaglobulinaemia	Inferred relationship	Existential restriction modifier (core metadata concept)
syndrome d'hyperimmunoglobulinémie E	Is a	False	Congenital hypergammaglobulinaemia	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets