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254287005: FRAXA (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2023. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    378521015 FRAXA en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    645159015 FRAXA (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    378521015 FRAXA en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    645159015 FRAXA (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    645159015 FRAXA (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    5083581000241110 fraxa fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    5083581000241110 fraxa fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    fraxa Is a Fragile X chromosome false Inferred relationship Existential restriction modifier (core metadata concept)
    fraxa Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    fraxa Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    fraxa Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
    fraxa Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
    fraxa Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    fraxa Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    fraxa Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
    fraxa Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    fraxa Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier (core metadata concept) 1
    fraxa Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    fraxa Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    fraxa Associated morphology Chromosomal morphology (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    fraxa Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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