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72682008: Isolated xanthine oxidase deficiency (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2023. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    120732016 Isolated xanthine oxidase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    120734015 Hereditary xanthinuria, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    812986018 Isolated xanthine oxidase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    13979261000172119 forme classique de la xanthinurie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
    13979271000172111 déficit isolé en xanthine oxydase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
    13979281000172114 xanthinurie héréditaire de type I fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
    4363101000172114 geïsoleerde deficiëntie van xanthineoxidase nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
    4363111000172112 geïsoleerde xanthineoxidasedeficiëntie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    déficit isolé en xanthine oxydase Is a Hereditary xanthinuria false Inferred relationship Some
    déficit isolé en xanthine oxydase Is a Autosomal recessive hereditary disorder false Inferred relationship Some
    déficit isolé en xanthine oxydase Occurrence Congenital false Inferred relationship Some
    déficit isolé en xanthine oxydase Finding site Body system structure false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    Description inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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