FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.7  |  FHIR Version n/a  User: [n/a]

1187119002: Hereditary pediatric Behçet-like disease (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2026. 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 Inactive 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 Inactive Entire term case sensitive (core metadata concept) 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 false Inferred relationship Some
    Hereditary paediatric Behçet-like disease Is a Inflammatory disorder false Inferred relationship Some
    Hereditary paediatric Behçet-like disease Is a Systemic disease false Inferred relationship Some
    Hereditary paediatric Behçet-like disease Is a Recurrent disease false Inferred relationship Some
    Hereditary paediatric Behçet-like disease Clinical course Recurrent false Inferred relationship Some 3
    Hereditary paediatric Behçet-like disease Associated morphology Inflammatory morphology (morphologic abnormality) false Inferred relationship Some 1
    Hereditary paediatric Behçet-like disease Is a Haploinsufficiency of A20 false Inferred relationship Some
    Hereditary paediatric Behçet-like disease Is a Hereditary disorder of immune system false Inferred relationship Some
    Hereditary paediatric Behçet-like disease Finding site Structure of immune system (body structure) false Inferred relationship Some 2
    Hereditary paediatric Behçet-like disease Associated morphology Inflammatory morphology (morphologic abnormality) false Inferred relationship Some 2
    Hereditary paediatric Behçet-like disease Pathological process (attribute) Abnormal immune process (qualifier value) false Inferred relationship Some 2

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

    Back to Start