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197478000: Congenital celiac disease (disorder)

    Status: retired, Primitive. Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    303685014 Congenital celiac disease en Synonym Active Case insensitive SNOMED CT core
    303686010 Congenital coeliac disease en Synonym Active Case insensitive SNOMED CT core
    581861015 Congenital celiac disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital coeliac disease Pathological process Pathological developmental process false Inferred relationship Some 3
    Congenital coeliac disease Has definitional manifestation Decreased hormone secretion false Inferred relationship Some
    Congenital coeliac disease Finding site Entire endocrine gonad false Inferred relationship Some
    Congenital coeliac disease Finding site Gonadal endocrine structure false Inferred relationship Some 4
    Congenital coeliac disease Is a Congenital disease false Inferred relationship Some
    Congenital coeliac disease Occurrence Congenital false Inferred relationship Some
    Congenital coeliac disease Is a Coeliac infantilism false Inferred relationship Some
    Congenital coeliac disease Occurrence Congenital false Inferred relationship Some 1
    Congenital coeliac disease Finding site Structure of small intestine false Inferred relationship Some 1
    Congenital coeliac disease Finding site Structure of small intestine false Inferred relationship Some
    Congenital coeliac disease Finding site Gonadal structure false Inferred relationship Some
    Congenital coeliac disease Causative agent Gluten false Inferred relationship Some 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    POSSIBLY EQUIVALENT TO association reference set

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