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237915001: Homogentisic acid defect (disorder)


    Status: retired, Primitive. Date: 31-Jul 2004. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    356574018 Homogentisic acid defect en Synonym Active Case insensitive SNOMED CT core
    626715016 Homogentisic acid defect (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
    Homogentisic acid defect Is a Disorder of tyrosine metabolism false Inferred relationship Some
    Homogentisic acid defect Finding site Body system structure false Inferred relationship Some
    Homogentisic acid defect Occurrence Congenital false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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