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56588001: Congenital hyperpigmentation (morphologic abnormality)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    94104017 Congenital hyperpigmentation en Synonym Active Entire term case insensitive SNOMED CT core module
    795116010 Congenital hyperpigmentation (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Congenital hyperpigmentation Is a Congenital pigmentation false Inferred relationship Existential restriction modifier
    Congenital hyperpigmentation Is a Hyperpigmentation false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Congenital melanosis of sclera Associated morphology False Congenital hyperpigmentation Inferred relationship Existential restriction modifier 2
    Congenital melanosis Associated morphology False Congenital hyperpigmentation Inferred relationship Existential restriction modifier 2
    Neuroectodermal melanolysosomal disease Associated morphology False Congenital hyperpigmentation Inferred relationship Existential restriction modifier 3
    Carney complex Associated morphology False Congenital hyperpigmentation Inferred relationship Existential restriction modifier 5
    Carney complex, trismus, pseudocamptodactyly syndrome Associated morphology False Congenital hyperpigmentation Inferred relationship Existential restriction modifier 2

    This concept is not in any reference sets

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