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82286005: Hyperimmunoglobulin M syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1216993016 Immunodeficiency with IgM hypergammaglobulinaemia en Synonym Active Initial character case insensitive SNOMED CT core
1218484015 Immunodeficiency with IgM hypergammaglobulinemia en Synonym Active Initial character case insensitive SNOMED CT core
1234699010 Hyper IgM syndrome en Synonym Active Initial character case insensitive SNOMED CT core
136491010 Hyperimmunoglobulin M syndrome en Synonym Active Initial character case insensitive SNOMED CT core
823676012 Hyperimmunoglobulin M syndrome (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyper IgM syndrome Pathological process Abnormal immune process true Inferred relationship Some 2
Hyper IgM syndrome Has definitional manifestation Immune system finding false Inferred relationship Some
Hyper IgM syndrome Is a Congenital hypergammaglobulinaemia true Inferred relationship Some
Hyper IgM syndrome Finding site Structure of immune system false Inferred relationship Some
Hyper IgM syndrome Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Hyperimmunoglobulin M syndrome with susceptibility to opportunistic infection Is a True Hyper IgM syndrome Inferred relationship Some
Hyperimmunoglobulin M syndrome without susceptibility to opportunistic infection Is a True Hyper IgM syndrome Inferred relationship Some
X-linked hyper-IgM syndrome Is a True Hyper IgM syndrome Inferred relationship Some
Autosomal recessive hyper-IgM syndrome Is a True Hyper IgM syndrome Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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