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237915001: Homogentisic acid defect (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2004. Module: SNOMED CT core module

    Descriptions:

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

    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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