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204963007: Other specified congenital cystic kidney disease (disorder)


    Status: retired, Primitive. Date: 31-Jan 2010. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    314302019 Other specified congenital cystic kidney disease en Synonym Active Case insensitive SNOMED CT core
    590263018 Other specified congenital cystic kidney disease (disorder) en Fully specified name Active Case insensitive SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Other specified congenital cystic kidney disease Finding site Urinary system structure false Inferred relationship Some 9
    Other specified congenital cystic kidney disease Occurrence Congenital false Inferred relationship Some
    Other specified congenital cystic kidney disease Associated morphology Fibrocystic change false Inferred relationship Some 1
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
    Other specified congenital cystic kidney disease Course Multiple superficial injuries of lower leg false Inferred relationship Some
    Other specified congenital cystic kidney disease Associated morphology Congenital anomaly false Inferred relationship Some 1
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
    Other specified congenital cystic kidney disease Associated morphology Fibrocystic change false Inferred relationship Some 2
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 1
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
    Other specified congenital cystic kidney disease Associated morphology Polycystic change false Inferred relationship Some 2
    Other specified congenital cystic kidney disease Finding site Kidney structure false Inferred relationship Some 2
    Other specified congenital cystic kidney disease Is a Polycystic kidney disease false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Other congenital cystic kidney disease NOS Is a False Other specified congenital cystic kidney disease Inferred relationship Some
    Congenital cystic kidney disease NOS Is a False Other specified congenital cystic kidney disease Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    WAS A association reference set

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