7251000146109: hyper-IgM-syndroom type 5 (aandoening)

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

\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Autosomal recessive hyperimmunoglobulin M syndrome (disorder)\Hyperimmunoglobulin M syndrome type 5 (disorder)

\Disorder of immune function (disorder)\Immunodeficiency disorder\Congenital immunodeficiency disease\Congenital hypergammaglobulinaemia\Hyperimmunoglobulin M syndrome\Autosomal recessive hyperimmunoglobulin M syndrome (disorder)\Hyperimmunoglobulin M syndrome type 5 (disorder)

\Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital immunodeficiency disease\Congenital hypergammaglobulinaemia\Hyperimmunoglobulin M syndrome\Autosomal recessive hyperimmunoglobulin M syndrome (disorder)\Hyperimmunoglobulin M syndrome type 5 (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2015. Module: SNOMED CT Netherlands NRC maintained module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

23441000146112 Hyperimmunoglobulin M syndrome type 5 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

23451000146110 Hyperimmunoglobulin M syndrome type 5 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

23461000146113 Hyper IgM syndrome type 5 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

27841000146117 hyper-IgM-syndroom type 5 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

395631000146111 UNG-deficiëntie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

4191401000146119 hyper-IgM-syndroom type 5 (aandoening) nl Fully specified name Active Only initial character 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
Hyperimmunoglobulin M syndrome type 5 (disorder)	Is a	Hyperimmunoglobulin M syndrome	false	Inferred relationship	Some
Hyperimmunoglobulin M syndrome type 5 (disorder)	Has definitional manifestation	Immune system finding	false	Inferred relationship	Some
Hyperimmunoglobulin M syndrome type 5 (disorder)	Occurrence	Congenital	false	Inferred relationship	Some
Hyperimmunoglobulin M syndrome type 5 (disorder)	Interprets	Globulin measurement (procedure)	false	Inferred relationship	Some
Hyperimmunoglobulin M syndrome type 5 (disorder)	Finding site	Structure of immune system (body structure)	false	Inferred relationship	Some
Hyperimmunoglobulin M syndrome type 5 (disorder)	Is a	Autosomal recessive hyperimmunoglobulin M syndrome	false	Inferred relationship	Some
Hyperimmunoglobulin M syndrome type 5 (disorder)	Has definitional manifestation	Immune system finding	false	Inferred relationship	Some
Hyperimmunoglobulin M syndrome type 5 (disorder)	Is a	Autosomal recessive hyperimmunoglobulin M syndrome (disorder)	true	Inferred relationship	Some
Hyperimmunoglobulin M syndrome type 5 (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	2
Hyperimmunoglobulin M syndrome type 5 (disorder)	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets