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56588001: Congenital hyperpigmentation (morphologic abnormality)

    Status: retired, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    795116010 Congenital hyperpigmentation (morphologic abnormality) en Fully specified name Active Case insensitive SNOMED CT core
    94104017 Congenital hyperpigmentation en Synonym Active Case insensitive 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
    Neuroectodermal melanolysosomal disease Associated morphology False Congenital hyperpigmentation Inferred relationship Some 3
    Carney complex Associated morphology False Congenital hyperpigmentation Inferred relationship Some 5
    Congenital melanosis of sclera Associated morphology False Congenital hyperpigmentation Inferred relationship Some 2
    Congenital melanosis Associated morphology False Congenital hyperpigmentation Inferred relationship Some 2
    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

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