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307360006: Leucodystrophy without a known biochemical basis (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    2816337016 Leukodystrophy without a known biochemical basis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    450606017 Leucodystrophy without a known biochemical basis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    703875019 Leucodystrophy without a known biochemical basis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Leucodystrophy without a known biochemical basis est un(e) (attribut) Leukodystrophy (disorder) false Inferred relationship Some
    Leucodystrophy without a known biochemical basis est un(e) (attribut) System disorder of the nervous system (disorder) false Inferred relationship Some
    Leucodystrophy without a known biochemical basis est un(e) (attribut) Hereditary disorder of nervous system false Inferred relationship Some
    Leucodystrophy without a known biochemical basis est un(e) (attribut) Leukodystrophy false Inferred relationship Some
    Leucodystrophy without a known biochemical basis morphologie associée (attribut) Myelin sheath alteration false Inferred relationship Some 1
    Leucodystrophy without a known biochemical basis morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 1
    Leucodystrophy without a known biochemical basis morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 1
    Leucodystrophy without a known biochemical basis localisation d'une constatation (attribut) système nerveux false Inferred relationship Some 1
    Leucodystrophy without a known biochemical basis morphologie associée (attribut) Myelin sheath alteration false Inferred relationship Some 1
    Leucodystrophy without a known biochemical basis localisation d'une constatation (attribut) système nerveux false Inferred relationship Some 1
    Leucodystrophy without a known biochemical basis survenue (attribut) congénital false Inferred relationship Some
    Leucodystrophy without a known biochemical basis localisation d'une constatation (attribut) White matter structure of brain and spinal cord (body structure) false Inferred relationship Some 2
    Leucodystrophy without a known biochemical basis morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 2
    Leucodystrophy without a known biochemical basis localisation d'une constatation (attribut) Myelinated nerve fiber structure false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Schultz disease est un(e) (attribut) False Leucodystrophy without a known biochemical basis Inferred relationship Some
    Pelizaeus-Merzbacher disease est un(e) (attribut) False Leucodystrophy without a known biochemical basis Inferred relationship Some
    Alexander's disease est un(e) (attribut) False Leucodystrophy without a known biochemical basis Inferred relationship Some

    Reference Sets

    Canada English language reference set (foundation metadata concept)

    Concept inactivation indicator reference set

    GB English

    US English

    REPLACED BY association reference set (foundation metadata concept)

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