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307360006: Leucodystrophy without a known biochemical basis (disorder)

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

    Descriptions:

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

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Leucodystrophy without a known biochemical basis Is a Leukodystrophy false Inferred relationship Existential restriction modifier
    Leucodystrophy without a known biochemical basis Is a System disorder of the nervous system false Inferred relationship Existential restriction modifier
    Leucodystrophy without a known biochemical basis Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
    Leucodystrophy without a known biochemical basis Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 1
    Leucodystrophy without a known biochemical basis Occurrence Congenital false Inferred relationship Existential restriction modifier
    Leucodystrophy without a known biochemical basis Is a Leukodystrophy false Inferred relationship Existential restriction modifier
    Leucodystrophy without a known biochemical basis Associated morphology Myelin sheath alteration false Inferred relationship Existential restriction modifier 1
    Leucodystrophy without a known biochemical basis Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 1
    Leucodystrophy without a known biochemical basis Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 1
    Leucodystrophy without a known biochemical basis Finding site Structure of nervous system false Inferred relationship Existential restriction modifier 1
    Leucodystrophy without a known biochemical basis Associated morphology Myelin sheath alteration false Inferred relationship Existential restriction modifier 1
    Leucodystrophy without a known biochemical basis Finding site White matter structure of brain and spinal cord false Inferred relationship Existential restriction modifier 2
    Leucodystrophy without a known biochemical basis Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 2
    Leucodystrophy without a known biochemical basis Finding site Myelinated nerve fiber structure false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Schultz disease Is a False Leucodystrophy without a known biochemical basis Inferred relationship Existential restriction modifier
    Pelizaeus-Merzbacher disease Is a False Leucodystrophy without a known biochemical basis Inferred relationship Existential restriction modifier
    Alexander's disease Is a False Leucodystrophy without a known biochemical basis Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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