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724205009: Laminopathy type Decaudain Vigouroux (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    3481698017 Laminopathy type Decaudain Vigouroux (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
    3481699013 Laminopathy type Decaudain Vigouroux en Synonym Active Only initial character case insensitive SNOMED CT core module
    3481700014 Laminopathy with severe metabolic syndrome and myopathy 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
    Laminopathy type Decaudain Vigouroux Due to Genetic syndrome false Inferred relationship Existential restriction modifier
    Laminopathy type Decaudain Vigouroux Is a Diabetes mellitus associated with genetic syndrome false Inferred relationship Existential restriction modifier
    Laminopathy type Decaudain Vigouroux Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
    Laminopathy type Decaudain Vigouroux Is a Hereditary disorder of endocrine system false Inferred relationship Existential restriction modifier
    Laminopathy type Decaudain Vigouroux Is a Diabetes mellitus due to genetic defect in insulin action false Inferred relationship Existential restriction modifier
    Laminopathy type Decaudain Vigouroux Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Laminopathy type Decaudain Vigouroux Finding site Structure of endocrine system false Inferred relationship Existential restriction modifier 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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