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52692001: Albinoidism (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    87685011 Albinoidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    790729018 Albinoidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    1453091000005111 Albinoidisme da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) dansk modul

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Albinoidisme Is a Albinism false Inferred relationship Some
    Albinoidisme Associated morphology Kongenit hypopigmentering false Inferred relationship Some 1
    Albinoidisme Finding site Skin structure false Inferred relationship Some 3
    Albinoidisme Finding site Eye structure false Inferred relationship Some
    Albinoidisme Occurrence Congenital false Inferred relationship Some
    Albinoidisme Finding site Structure of skin region false Inferred relationship Some 1
    Albinoidisme Associated morphology kongenit mangel false Inferred relationship Some
    Albinoidisme Finding site Eye region structure (body structure) false Inferred relationship Some
    Albinoidisme Associated morphology Kongenit hypopigmentering false Inferred relationship Some 1
    Albinoidisme Finding site Eye structure false Inferred relationship Some 2
    Albinoidisme Is a Site-specific disorder of skin false Inferred relationship Some
    Albinoidisme Is a Hereditary disorder of the integument false Inferred relationship Some
    Albinoidisme Is a Hereditary disorder of the visual system (disorder) false Inferred relationship Some
    Albinoidisme Is a Disorder of tyrosine metabolism false Inferred relationship Some
    Albinoidisme Is a Congenital deficiency of pigment of skin false Inferred relationship Some
    Albinoidisme Is a Disorder of eye region (disorder) false Inferred relationship Some
    Albinoidisme Associated morphology Decreased melanin pigmentation false Inferred relationship Some
    Albinoidisme Finding site Eye region structure (body structure) false Inferred relationship Some
    Albinoidisme Finding site Skin structure false Inferred relationship Some 1
    Albinoidisme Finding site Skin structure false Inferred relationship Some 1
    Albinoidisme Associated morphology Kongenit hypopigmentering false Inferred relationship Some 1
    Albinoidisme Occurrence Congenital false Inferred relationship Some 2
    Albinoidisme Associated morphology Kongenit hypopigmentering false Inferred relationship Some 2
    Albinoidisme Finding site Skin structure false Inferred relationship Some 2
    Albinoidisme Occurrence Congenital false Inferred relationship Some 3
    Albinoidisme Associated morphology Decreased melanin pigmentation false Inferred relationship Some 3
    Albinoidisme Is a Genetic disorder of skin pigmentation (disorder) false Inferred relationship Some
    Albinoidisme Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Albinoidisme Occurrence Congenital false Inferred relationship Some 1
    Albinoidisme Associated morphology Hypopigmentation false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Okulokutan albinoidisme Is a False Albinoidisme Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    US English

    SAME AS association reference set (foundation metadata concept)

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