119021000146105: hereditaire hypogammaglobulinemie (aandoening)

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

\Procedure related finding\Evaluation finding\Measurement finding\...

\Finding of substance level (finding)\Protein level - finding\Globulin level - finding\Globulin level outside reference range (finding)\Globulin below reference range\Hypogammaglobulinemia\Hereditary hypogammaglobulinemia (disorder)

\Measurement finding outside reference range\Measurement finding below reference range (finding)\Globulin below reference range\Hypogammaglobulinemia\Hereditary hypogammaglobulinemia (disorder)
\Measurement finding outside reference range\Globulin level outside reference range (finding)\Globulin below reference range\Hypogammaglobulinemia\Hereditary hypogammaglobulinemia (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary hypogammaglobulinemia (disorder)
\Disease\Disorder of immune function (disorder)\Hereditary disorder of immune system\Hereditary hypogammaglobulinemia (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary hypogammaglobulinemia (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2020. Module: SNOMED CT Netherlands NRC maintained module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

9234731000146111 Hereditary hypogammaglobulinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
9234741000146115 Hereditary hypogammaglobulinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10597511000146115 erfelijke hypogammaglobulinemie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10868291000146113 hereditaire hypogammaglobulinemie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10868301000146112 hereditaire hypogammaglobulinemie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary hypogammaglobulinemia (disorder)	Is a	Hypogammaglobulinemia	true	Inferred relationship	Some
Hereditary hypogammaglobulinemia (disorder)	Is a	Hereditary disorder of immune system	true	Inferred relationship	Some
Hereditary hypogammaglobulinemia (disorder)	Finding site	Body system structure	true	Inferred relationship	Some	1
Hereditary hypogammaglobulinemia (disorder)	Interprets	Globulin measurement (procedure)	true	Inferred relationship	Some	3
Hereditary hypogammaglobulinemia (disorder)	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Some	2
Hereditary hypogammaglobulinemia (disorder)	Has interpretation	Below reference range	true	Inferred relationship	Some	3

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Osteopetrosis hypogammaglobulinemia syndrome (disorder)	Is a	True	Hereditary hypogammaglobulinemia (disorder)	Inferred relationship	Some

This concept is not in any reference sets