1187119002: Hereditary pediatric Behçet-like disease (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Monogenic autoinflammatory syndrome (disorder)\Haploinsufficiency of A20\Hereditary paediatric Behçet-like disease
• \Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary paediatric Behçet-like disease
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hereditary paediatric Behçet-like disease
• \Disorder of immune function (disorder)\Autoinflammatory disease (disorder)\Monogenic autoinflammatory syndrome (disorder)\Haploinsufficiency of A20\Hereditary paediatric Behçet-like disease
• \Disorder of immune function (disorder)\Hereditary disorder of immune system\Hereditary paediatric Behçet-like disease
• \Disorder of body system\Disorder of immune structure (disorder)\Inflammatory disorder of immune system\Autoinflammatory disease (disorder)\Monogenic autoinflammatory syndrome (disorder)\Haploinsufficiency of A20\Hereditary paediatric Behçet-like disease
• \Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of immune system\Autoinflammatory disease (disorder)\Monogenic autoinflammatory syndrome (disorder)\Haploinsufficiency of A20\Hereditary paediatric Behçet-like disease
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Hereditary paediatric Behçet-like disease
• \Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of immune system\Autoinflammatory disease (disorder)\Monogenic autoinflammatory syndrome (disorder)\Haploinsufficiency of A20\Hereditary paediatric Behçet-like disease
• \Recurrent disease\Hereditary paediatric Behçet-like disease
• \Systemic disease\Haploinsufficiency of A20\Hereditary paediatric Behçet-like disease

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4669941019	Behçet-like disease due to HA20	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4669942014	Hereditary paediatric Behçet-like disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4669943016	Hereditary pediatric Behçet-like disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4669944010	Hereditary pediatric Behçet-like disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4669945011	Behçet-like disease due to haploinsufficiency of A20	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4669946012	A rare autosomal dominant autoinflammatory syndrome characterized by early onset systemic inflammation with autoimmune manifestations and more rarely, humoral immune deficiency and increased production of circulating proinflammatory cytokines. Variable manifestations include recurrent oral aphthous ulcers, genital ulcers, arthralgia or arthritis, periodic fever, uveitis and severe gastrointestinal involvement (pain, diarrhea, vomiting, rectal bleeding).	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4669947015	A rare autosomal dominant autoinflammatory syndrome characterised by early onset systemic inflammation with autoimmune manifestations and more rarely, humoral immune deficiency and increased production of circulating proinflammatory cytokines. Variable manifestations include recurrent oral aphthous ulcers, genital ulcers, arthralgia or arthritis, periodic fever, uveitis and severe gastrointestinal involvement (pain, diarrhoea, vomiting, rectal bleeding).	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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