267460002: Congenital hypogammaglobulinemia (finding)

SNOMED CT Concept\Clinical finding (finding)\Procedure related finding\Evaluation finding\Measurement finding\...

\Finding of substance level (finding)\Finding of protein level (finding)\Globulin level - finding\Globulin level outside reference range (finding)\Globulin below reference range\Hypogammaglobulinemia\Congenital hypogammaglobulinaemia

\Measurement finding outside reference range\Measurement finding below reference range (finding)\Globulin below reference range\Hypogammaglobulinemia\Congenital hypogammaglobulinaemia
\Measurement finding outside reference range\Globulin level outside reference range (finding)\Globulin below reference range\Hypogammaglobulinemia\Congenital hypogammaglobulinaemia

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Dec 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

398903019 Congenital hypogammaglobulinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

398904013 Congenital hypogammaglobulinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

660080016 Congenital hypogammaglobulinemia (finding) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

398903019 Congenital hypogammaglobulinaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

398903019 Congenital hypogammaglobulinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

398904013 Congenital hypogammaglobulinemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

398904013 Congenital hypogammaglobulinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

660080016 Congenital hypogammaglobulinemia (finding) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

660080016 Congenital hypogammaglobulinemia (finding) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5107141000241113 hypogammaglobulinémie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5107141000241113 hypogammaglobulinémie 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 hypogammaglobulinaemia	Is a	Agammaglobulinemia	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hypogammaglobulinaemia	Finding site	Structure of immune system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypogammaglobulinaemia	Interprets	Biochemistry test interpretation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hypogammaglobulinaemia	Interprets	Laboratory test	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hypogammaglobulinaemia	Finding method	Procedure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hypogammaglobulinaemia	Interprets	Globulin measurement (procedure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hypogammaglobulinaemia	Interprets	Globulin measurement (procedure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypogammaglobulinaemia	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital hypogammaglobulinaemia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital hypogammaglobulinaemia	Is a	Hypogammaglobulinemia	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Osteopetrosis hypogammaglobulinemia syndrome (disorder)	Is a	True	Congenital hypogammaglobulinaemia	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets