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204742002: Hirschsprung's disease NOS (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2010. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    313960011 Hirschsprung's disease NOS en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    590009013 Hirschsprung's disease NOS (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    313960011 Hirschsprung's disease NOS en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    590009013 Hirschsprung's disease NOS (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    590009013 Hirschsprung's disease NOS (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hirschsprung's disease NOS Is a Congenital aganglionic megacolon (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Hirschsprung's disease NOS Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Hirschsprung's disease NOS Finding site Colon structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hirschsprung's disease NOS Finding site Autonomic nerve structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Hirschsprung's disease NOS Finding site Parasympathetic nervous system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Hirschsprung's disease NOS Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hirschsprung's disease NOS Finding site Structure of large intestine (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hirschsprung's disease NOS Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Hirschsprung's disease NOS Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hirschsprung's disease NOS Associated morphology hypertrophie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hirschsprung's disease NOS Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hirschsprung's disease NOS Finding site Colon structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hirschsprung's disease NOS Associated morphology hypertrophie congénitale 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)

    WAS A association reference set (foundation metadata concept)

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