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204742002: Hirschsprung's disease NOS (disorder)

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

    Descriptions:

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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hirschsprung's disease NOS Is a Hirschsprung's disease false Inferred relationship Existential restriction modifier
    Hirschsprung's disease NOS Occurrence Congenital false Inferred relationship Existential restriction modifier
    Hirschsprung's disease NOS Finding site Colon structure false Inferred relationship Existential restriction modifier 1
    Hirschsprung's disease NOS Finding site Autonomic nerve structure false Inferred relationship Existential restriction modifier
    Hirschsprung's disease NOS Finding site Parasympathetic nervous system structure false Inferred relationship Existential restriction modifier
    Hirschsprung's disease NOS Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Hirschsprung's disease NOS Finding site Structure of large intestine false Inferred relationship Existential restriction modifier 1
    Hirschsprung's disease NOS Occurrence Congenital false Inferred relationship Existential restriction modifier
    Hirschsprung's disease NOS Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier 1
    Hirschsprung's disease NOS Associated morphology Congenital hypertrophy false Inferred relationship Existential restriction modifier 1
    Hirschsprung's disease NOS Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier 1
    Hirschsprung's disease NOS Finding site Colon structure false Inferred relationship Existential restriction modifier 1
    Hirschsprung's disease NOS Associated morphology Congenital hypertrophy false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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