FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

204570003: Other specified congenital cystic lung (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
    313664017 Other specified congenital cystic lung en Synonym Active Entire term case insensitive SNOMED CT core module
    589813013 Other specified congenital cystic lung (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
    Other specified congenital cystic lung Is a Congenital cystic lung disease, unspecified false Inferred relationship Existential restriction modifier
    Other specified congenital cystic lung Associated morphology Congenital cavitation false Inferred relationship Existential restriction modifier 1
    Other specified congenital cystic lung Associated morphology Fibrocysticystic change (morphologic abnormality) false Inferred relationship Existential restriction modifier
    Other specified congenital cystic lung Finding site Lung structure false Inferred relationship Existential restriction modifier 1
    Other specified congenital cystic lung Occurrence Congenital false Inferred relationship Existential restriction modifier
    Other specified congenital cystic lung Finding site Lung structure false Inferred relationship Existential restriction modifier 1
    Other specified congenital cystic lung Associated morphology Congenital cavitation false Inferred relationship Existential restriction modifier 1

    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

    Back to Start