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55824003: Essential benign pentosuria (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2013. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    92832010 Essential benign pentosuria en Synonym Active Entire term case insensitive SNOMED CT core module
    92833017 Pentosuria en Synonym Active Entire term case insensitive SNOMED CT core module
    92834011 Xylitol dehydrogenase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
    92835012 L-xylulose reductase deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
    92836013 L-xylulosuria en Synonym Active Entire term case sensitive SNOMED CT core module
    794253018 Essential benign pentosuria (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
    Essential benign pentosuria Is a Enzymopathy false Inferred relationship Existential restriction modifier
    Essential benign pentosuria Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
    Essential benign pentosuria Is a Pentose disorder false Inferred relationship Existential restriction modifier
    Essential benign pentosuria Is a Inborn error of metabolism false Inferred relationship Existential restriction modifier
    Essential benign pentosuria Finding site Body system structure false Inferred relationship Existential restriction modifier
    Essential benign pentosuria 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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