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59379005: Congenital pigmentary anomaly of skin (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    98624012 Congenital pigmentary anomaly of skin en Synonym Active Entire term case insensitive SNOMED CT core module
    798214015 Congenital pigmentary anomaly of skin (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

    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
    Congenital pigmentary anomaly of skin Is a Congenital anomaly of skin false Inferred relationship Existential restriction modifier
    Congenital pigmentary anomaly of skin Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Congenital pigmentary anomaly of skin Associated morphology Congenital pigmentation false Inferred relationship Existential restriction modifier 1
    Congenital pigmentary anomaly of skin Occurrence Congenital false Inferred relationship Existential restriction modifier
    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

    This concept is not in any reference sets

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