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205568000: Congenital pigmentary skin anomaly NOS (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2010. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    315252018 Congenital pigmentary skin anomaly NOS en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    590954012 Congenital pigmentary skin anomaly NOS (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital pigmentary skin anomaly NOS Is a Congenital pigmentary skin anomalies false Inferred relationship Some
    Congenital pigmentary skin anomaly NOS Finding site Structure of skin region false Inferred relationship Some 1
    Congenital pigmentary skin anomaly NOS Associated morphology Congenital malformation false Inferred relationship Some
    Congenital pigmentary skin anomaly NOS Finding site Upper gastrointestinal tract structure false Inferred relationship Some
    Congenital pigmentary skin anomaly NOS Occurrence Congenital false Inferred relationship Some
    Congenital pigmentary skin anomaly NOS Associated morphology Congenital anomaly false Inferred relationship Some 1
    Congenital pigmentary skin anomaly NOS Finding site Jaw region structure false Inferred relationship Some
    Congenital pigmentary skin anomaly NOS Finding site Tongue structure false Inferred relationship Some 1
    Congenital pigmentary skin anomaly NOS Finding site Heart structure false Inferred relationship Some
    Congenital pigmentary skin anomaly NOS Associated morphology Congenital anomaly false Inferred relationship Some 2
    Congenital pigmentary skin anomaly NOS Finding site Cardiovascular system subdivision false Inferred relationship Some 2
    Congenital pigmentary skin anomaly NOS Associated morphology Pigment alteration false Inferred relationship Some 2
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Some 1
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Some 2
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Some 1
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Some 2
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Some 1
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Some 2
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Some 1
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Some 2

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    WAS A association reference set

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