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59379005: Congenital pigmentary anomaly of skin (disorder)


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

    Descriptions:

    Id Description Lang Type Status Case? Module
    98624012 Congenital pigmentary anomaly of skin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    798214015 Congenital pigmentary anomaly of skin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    98624012 Congenital pigmentary anomaly of skin en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    98624012 Congenital pigmentary anomaly of skin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    798214015 Congenital pigmentary anomaly of skin (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    798214015 Congenital pigmentary anomaly of skin (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
    Congenital pigmentary anomaly of skin Is a Skin lesion false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital pigmentary anomaly of skin Is a Congenital anomaly of skin (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Congenital pigmentary anomaly of skin Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital pigmentary anomaly of skin Associated morphology Congenital pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Congenital pigmentary anomaly of skin Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Congenital deficiency of pigment of skin Is a False Congenital pigmentary anomaly of skin Inferred relationship Existential restriction modifier (core metadata concept)

    Reference Sets

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

    SAME AS association reference set (foundation metadata concept)

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