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402777004: Hereditary lentiginosis (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    1770701018 Hereditary lentiginosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1781871010 Hereditary lentiginosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1770701018 Hereditary lentiginosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1770701018 Hereditary lentiginosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1781871010 Hereditary lentiginosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    1781871010 Hereditary lentiginosis en Synonym (core metadata concept) 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
    Hereditary lentiginosis Is a Congenital/hereditary lentiginosis false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary lentiginosis Is a lentigo false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary lentiginosis Is a Hereditary hypermelanosis (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary lentiginosis Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary lentiginosis Associated morphology Hyperpigmentation (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary lentiginosis Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hereditary lentiginosis Associated morphology Melanosis false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Hereditary lentiginosis Associated morphology Increased melanin pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
    Hereditary lentiginosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Generalized lentiginosis Is a False Hereditary lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)
    A rare association syndrome, reported in several members of two families to date, characterized by arterial dissection, occurring at an early age and presenting with a range of manifestations depending on the vascular territory involved (headache, dysphasia, hemiparesis), in association with cystic medial necrosis and multiple lentigines (brown and black in color and mainly affecting the skin of the trunk and extremities). Is a False Hereditary lentiginosis Inferred relationship Existential restriction modifier (core metadata concept)

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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