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205568000: Congenital pigmentary skin anomaly NOS (disorder)

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

    Descriptions:

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

    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 Existential restriction modifier
    Congenital pigmentary skin anomaly NOS Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
    Congenital pigmentary skin anomaly NOS Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
    Congenital pigmentary skin anomaly NOS Finding site Upper gastrointestinal tract structure false Inferred relationship Existential restriction modifier
    Congenital pigmentary skin anomaly NOS Occurrence Congenital false Inferred relationship Existential restriction modifier
    Congenital pigmentary skin anomaly NOS Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Congenital pigmentary skin anomaly NOS Finding site Jaw region structure false Inferred relationship Existential restriction modifier
    Congenital pigmentary skin anomaly NOS Finding site Tongue structure false Inferred relationship Existential restriction modifier 1
    Congenital pigmentary skin anomaly NOS Finding site Heart structure false Inferred relationship Existential restriction modifier
    Congenital pigmentary skin anomaly NOS Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
    Congenital pigmentary skin anomaly NOS Finding site Structure of cardiovascular system subdivision false Inferred relationship Existential restriction modifier 2
    Congenital pigmentary skin anomaly NOS Associated morphology Pigment alteration false Inferred relationship Existential restriction modifier 2
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Congenital pigmentary skin anomaly NOS Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Congenital pigmentary skin anomaly NOS Finding site Skin structure 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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