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1290916005: Haploinsufficiency of A20 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Nov 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5276585012 Haploinsufficiency of A20 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5276586013 Haploinsufficiency of A20 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5276587016 HA20 (haploinsufficiency A20) en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5276588014 A20 haploinsufficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Haploinsufficiency of A20 Is a Systemic disease true Inferred relationship Some
Haploinsufficiency of A20 Is a Monogenic autoinflammatory syndrome (disorder) true Inferred relationship Some
Haploinsufficiency of A20 Finding site Structure of immune system (body structure) true Inferred relationship Some 1
Haploinsufficiency of A20 Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Some 1
Haploinsufficiency of A20 Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary paediatric Behçet-like disease Is a True Haploinsufficiency of A20 Inferred relationship Some

This concept is not in any reference sets

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