FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

192784006: Metachromatic leucodystrophy (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    296972018 Metachromatic leukodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    296973011 Sulphatide lipidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    296974017 Sulfatide lipidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    296975016 Greenfield disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    296976015 Metachromatic leucodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    296977012 MLD en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    296978019 Familial progressive cerebral sclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    296979010 van Bogaert-Nijssen disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    296980013 MLD - Metachromatic leucodystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    296981012 Metachromatic leukoencephaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    576603011 Metachromatic leucodystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    296972018 Metachromatic leukodystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    296972018 Metachromatic leukodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    296973011 Sulphatide lipidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    296973011 Sulphatide lipidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    296974017 Sulfatide lipidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    296974017 Sulfatide lipidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    296975016 Greenfield disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    296976015 Metachromatic leucodystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    296976015 Metachromatic leucodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    296977012 MLD en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    296978019 Familial progressive cerebral sclerosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    296978019 Familial progressive cerebral sclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    296979010 van Bogaert-Nijssen disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    296980013 MLD - Metachromatic leucodystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    296981012 Metachromatic leukoencephaly en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    296981012 Metachromatic leukoencephaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    576603011 Metachromatic leucodystrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    576603011 Metachromatic leucodystrophy (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
    Metachromatic leucodystrophy Is a Sphingolipidosis false Inferred relationship Existential restriction modifier (core metadata concept)
    Metachromatic leucodystrophy Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Metachromatic leucodystrophy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Arylsulfatase A deficiency Is a False Metachromatic leucodystrophy Inferred relationship Existential restriction modifier (core metadata concept)
    Metachromatic leukodystrophy due to deficiency of cerebroside sulfatase activator Is a False Metachromatic leucodystrophy Inferred relationship Existential restriction modifier (core metadata concept)
    Metachromatic leukodystrophy, congenital type Is a False Metachromatic leucodystrophy Inferred relationship Existential restriction modifier (core metadata concept)
    Sphingolipid activator protein 1 deficiency Is a False Metachromatic leucodystrophy Inferred relationship Existential restriction modifier (core metadata concept)
    Metachromatic leukodystrophy without arylsulfatase deficiency Is a False Metachromatic leucodystrophy Inferred relationship Existential restriction modifier (core metadata concept)

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

    Back to Start