FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

11606009: Gangrenous omphalocele (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    20057018 Gangrenous omphalocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    674581019 Gangrenous omphalocele (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    20057018 Gangrenous omphalocele en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    20057018 Gangrenous omphalocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    674581019 Gangrenous omphalocele (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    674581019 Gangrenous omphalocele (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Gangrenous omphalocele Is a Congenital anomaly of small intestine false Inferred relationship Existential restriction modifier (core metadata concept)
    Gangrenous omphalocele Is a Congenital anomaly of lower alimentary tract false Inferred relationship Existential restriction modifier (core metadata concept)
    Gangrenous omphalocele Is a Congenital omphalocele false Inferred relationship Existential restriction modifier (core metadata concept)
    Gangrenous omphalocele Associated morphology Congenital failure of fusion false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Gangrenous omphalocele Associated morphology Gangrene false Inferred relationship Existential restriction modifier (core metadata concept)
    Gangrenous omphalocele Associated morphology Congenital protrusion false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Gangrenous omphalocele Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Gangrenous omphalocele Finding site Umbilical structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Gangrenous omphalocele Finding site Jejunum, ileum, colon, rectum, and anal canal false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Gangrenous omphalocele Finding site Structure of small intestine (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Gangrenous omphalocele Finding site paroi abdominale false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Gangrenous omphalocele Is a Disorder of body wall and cavities false Inferred relationship Existential restriction modifier (core metadata concept)
    Gangrenous omphalocele Is a Gangrenous disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    Gangrenous omphalocele Finding site Structure of digestive system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    SAME AS association reference set (foundation metadata concept)

    Back to Start