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55824003: Essential benign pentosuria (disorder)

    Status: retired, Primitive. Date: 31-Jul 2013. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    794253018 Essential benign pentosuria (disorder) en Fully specified name Active Case insensitive SNOMED CT core
    92832010 Essential benign pentosuria en Synonym Active Case insensitive SNOMED CT core
    92833017 Pentosuria en Synonym Active Case insensitive SNOMED CT core
    92834011 Xylitol dehydrogenase deficiency en Synonym Active Case sensitive SNOMED CT core
    92835012 L-xylulose reductase deficiency en Synonym Active Case sensitive SNOMED CT core
    92836013 L-xylulosuria en Synonym Active Case sensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Essential benign pentosuria Is a Enzymopathy false Inferred relationship Some
    Essential benign pentosuria Is a Autosomal recessive hereditary disorder false Inferred relationship Some
    Essential benign pentosuria Is a Pentose disorder false Inferred relationship Some
    Essential benign pentosuria Is a Inborn error of metabolism false Inferred relationship Some
    Essential benign pentosuria Finding site Body system structure false Inferred relationship Some
    Essential benign pentosuria 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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