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1187119002: Hereditary pediatric Behçet-like disease (disorder)


Status: current, Primitive. 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 Active Case sensitive SNOMED CT core
4669942014 Hereditary paediatric Behçet-like disease en Synonym Active Initial character case insensitive SNOMED CT core
4669943016 Hereditary pediatric Behçet-like disease en Synonym Active Initial character case insensitive SNOMED CT core
4669944010 Hereditary pediatric Behçet-like disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
4669945011 Behçet-like disease due to haploinsufficiency of A20 en Synonym Active Case sensitive 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 Case sensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary paediatric Behçet-like disease Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hereditary paediatric Behçet-like disease Is a Inflammatory disorder true Inferred relationship Some
Hereditary paediatric Behçet-like disease Is a Systemic disease true Inferred relationship Some
Hereditary paediatric Behçet-like disease Is a Recurrent disease true Inferred relationship Some
Hereditary paediatric Behçet-like disease Clinical course Recurrent true Inferred relationship Some 3
Hereditary paediatric Behçet-like disease Associated morphology Inflammatory morphology true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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