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56588001: Congenital hyperpigmentation (morphologic abnormality)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    94104017 Congenital hyperpigmentation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    795116010 Congenital hyperpigmentation (morphologic abnormality) 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 hyperpigmentation Is a Congenital pigmentation false Inferred relationship Some
    Congenital hyperpigmentation Is a Hyperpigmentation false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Congenital melanosis of sclera Associated morphology False Congenital hyperpigmentation Inferred relationship Some 2
    Congenital melanosis Associated morphology False Congenital hyperpigmentation Inferred relationship Some 2
    Neuroectodermal melanolysosomal disease (disorder) Associated morphology False Congenital hyperpigmentation Inferred relationship Some 3
    Carney complex (disorder) Associated morphology False Congenital hyperpigmentation Inferred relationship Some 5
    Carney complex, trismus, pseudocamptodactyly syndrome Associated morphology False Congenital hyperpigmentation Inferred relationship Some 2

    Reference Sets

    Concept inactivation indicator reference set

    SAME AS association reference set (foundation metadata concept)

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