1187119002: Hereditary pediatric Behçet-like disease (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary pediatric Behçet-like disease
• \Inflammatory disorder\Hereditary pediatric Behçet-like disease
• \Recurrent disease\Hereditary pediatric Behçet-like disease
• \Systemic disease\Hereditary pediatric Behçet-like disease

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Nov 2021. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4669941019	Behçet-like disease due to HA20	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
4669942014	Hereditary paediatric Behçet-like disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4669943016	Hereditary pediatric Behçet-like disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4669944010	Hereditary pediatric Behçet-like disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
4669945011	Behçet-like disease due to haploinsufficiency of A20	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

Back to Start