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254238008: Familial focal facial dermal dysplasia (disorder)


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

    Descriptions:

    Id Description Lang Type Status Case? Module
    378467018 Familial focal facial dermal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    378468011 Brauer's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    645101010 Familial focal facial dermal dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    378467018 Familial focal facial dermal dysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    378467018 Familial focal facial dermal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    378468011 Brauer's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    645101010 Familial focal facial dermal dysplasia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    645101010 Familial focal facial dermal dysplasia (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
    Familial focal facial dermal dysplasia Is a Genodermatosis false Inferred relationship Existential restriction modifier (core metadata concept)
    Familial focal facial dermal dysplasia Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Familial focal facial dermal dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Familial focal facial dermal dysplasia Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Familial focal facial dermal dysplasia Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Familial focal facial dermal dysplasia Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Familial focal facial dermal dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Familial focal facial dermal dysplasia Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Familial focal facial dermal dysplasia Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Familial focal facial dermal dysplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Familial focal facial dermal dysplasia Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Familial focal facial dermal dysplasia Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Congenital ectodermal dysplasia of face Is a False Familial focal facial dermal dysplasia 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

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