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402777004: Hereditary lentiginosis (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    1770701018 Hereditary lentiginosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
    1781871010 Hereditary lentiginosis en Synonym Active Entire term case insensitive SNOMED CT core module

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hereditary lentiginosis Is a Congenital/hereditary lentiginosis false Inferred relationship Existential restriction modifier
    Hereditary lentiginosis Is a Lentigo false Inferred relationship Existential restriction modifier
    Hereditary lentiginosis Is a Hereditary hypermelanosis false Inferred relationship Existential restriction modifier
    Hereditary lentiginosis Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
    Hereditary lentiginosis Associated morphology Hyperpigmentation false Inferred relationship Existential restriction modifier 1
    Hereditary lentiginosis Occurrence Congenital false Inferred relationship Existential restriction modifier
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Hereditary lentiginosis Associated morphology Melanosis false Inferred relationship Existential restriction modifier 3
    Hereditary lentiginosis Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier 2
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 3
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 3
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 3
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier 3
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Generalized lentiginosis Is a False Hereditary lentiginosis Inferred relationship Existential restriction modifier
    Arterial dissection and lentiginosis syndrome Is a False Hereditary lentiginosis Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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