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1362020006: Hyperimmunoglobulin M syndrome type 3 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5443852012 Hyperimmunoglobulin M syndrome type 3 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5443853019 HIGM3 - hyperimmunoglobulin M syndrome type 3 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5443854013 Hyper-IgM syndrome due to CD40 deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5443855014 Hyperimmunoglobulin M syndrome type 3 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5443856010 Autosomal recessive combined immunodeficiency due to CD40 mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperimmunoglobulin M syndrome type 3 Is a Autosomal recessive hyperimmunoglobulin M syndrome (disorder) true Inferred relationship Some
Hyperimmunoglobulin M syndrome type 3 Is a Hyperimmunoglobulin M syndrome with susceptibility to opportunistic infection true Inferred relationship Some
Hyperimmunoglobulin M syndrome type 3 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

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