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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
    1734761000005112 Kongenitte hudpigmentanomalier, ikke nærmere specificeret da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Is a Congenital pigmentary skin anomalies false Inferred relationship Some
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Finding site Structure of skin region false Inferred relationship Some 1
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Associated morphology Kongenit malformation false Inferred relationship Some
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Finding site Esophagus, stomach, and duodenum. false Inferred relationship Some
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Occurrence Congenital false Inferred relationship Some
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Associated morphology kongenit anomali false Inferred relationship Some 1
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Finding site Jaw region structure false Inferred relationship Some
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Finding site Tongue structure false Inferred relationship Some 1
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Finding site Heart structure false Inferred relationship Some
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Associated morphology kongenit anomali false Inferred relationship Some 2
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Finding site Cardiovascular system subdivision false Inferred relationship Some 2
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Associated morphology Pigment alteration false Inferred relationship Some 2
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Finding site Skin structure false Inferred relationship Some 1
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Finding site Skin structure false Inferred relationship Some 2
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Finding site Skin structure false Inferred relationship Some 1
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Finding site Skin structure false Inferred relationship Some 2
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Finding site Skin structure false Inferred relationship Some 1
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Finding site Skin structure false Inferred relationship Some 2
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret Finding site Skin structure false Inferred relationship Some 1
    Kongenitte hudpigmentanomalier, ikke nærmere specificeret 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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