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286910004: Hypothyroidism - congenital and acquired (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    426396014 Hypothyroidism - congenital and acquired en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    681078012 Hypothyroidism - congenital and acquired (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    426396014 Hypothyroidism - congenital and acquired en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    426396014 Hypothyroidism - congenital and acquired en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    681078012 Hypothyroidism - congenital and acquired (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    681078012 Hypothyroidism - congenital and acquired (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    301721000077116 hypothyroïdie congénitale et acquise fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    301721000077116 hypothyroïdie congénitale et acquise 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
    hypothyroïdie congénitale et acquise Is a Hypothyroidism false Inferred relationship Existential restriction modifier (core metadata concept)
    hypothyroïdie congénitale et acquise Finding site Thyroid structure false Inferred relationship Existential restriction modifier (core metadata concept)
    hypothyroïdie congénitale et acquise Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
    hypothyroïdie congénitale et acquise Is a Congenital disease false Inferred relationship Existential restriction modifier (core metadata concept)
    hypothyroïdie congénitale et acquise Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    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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