FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

197478000: Congenital celiac disease (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

    Descriptions:

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

    0 descendants.

    Expanded Value Set

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

    This concept is not in any reference sets

    Back to Start