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192783000: Schultz disease (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    296970014 Schulz's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    296971013 Schultz disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    576602018 Schultz disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
    296970014 Schulz's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    296971013 Schultz disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    576602018 Schultz disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    576602018 Schultz disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Schultz disease Is a Leucodystrophy without a known biochemical basis false Inferred relationship Existential restriction modifier (core metadata concept)
    Schultz disease Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Schultz disease Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Schultz disease Associated morphology Myelin sheath alteration false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Schultz disease Associated morphology Dystrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Schultz disease Associated morphology Myelin sheath alteration false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Schultz disease Associated morphology Dystrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Schultz disease Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    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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