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5101009: Leukodystrophy (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2004. Module: SNOMED CT core module

    Descriptions:

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

    0 descendants.

    Expanded Value Set

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

    This concept is not in any reference sets

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