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5101009: Leukodystrophy (disorder)

    Status: retired, Primitive. Date: 31-Jul 2004. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    788863011 Leukodystrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
    9536012 Leukodystrophy en Synonym Active Case insensitive SNOMED CT core
    9537015 Leukodystrophy, NOS en Synonym Inactive Initial character case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Leukodystrophy Is a Disorder of lysosomal enzyme false Inferred relationship Some
    Leukodystrophy Finding site Body system structure false Inferred relationship Some
    Leukodystrophy Occurrence Congenital false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Leucodystrophy without a known biochemical basis Is a False Leukodystrophy Inferred relationship Some
    Galactosylceramide beta-galactosidase deficiency Is a False Leukodystrophy Inferred relationship Some
    Globoid cell leucodystrophy, late-onset Is a False Leukodystrophy Inferred relationship Some
    Dalmatian leukodystrophy Is a False Leukodystrophy Inferred relationship Some
    Neuroaxonal leucodystrophy Is a False Leukodystrophy Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set

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