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79417003: Autosomal dominant oculocutaneous albinism (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
    131767016 Autosomal dominant oculocutaneous albinism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    820465019 Autosomal dominant oculocutaneous albinism (disorder) en Fully specified name 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
    Autosomal dominant oculocutaneous albinism Is a Oculocutaneous albinism false Inferred relationship Some
    Autosomal dominant oculocutaneous albinism Is a Autosomal dominant hereditary disorder false Inferred relationship Some
    Autosomal dominant oculocutaneous albinism Associated morphology congenitale hypopigmentatie false Inferred relationship Some 2
    Autosomal dominant oculocutaneous albinism Finding site Skin structure false Inferred relationship Some 3
    Autosomal dominant oculocutaneous albinism Associated morphology Congenital deficiency false Inferred relationship Some
    Autosomal dominant oculocutaneous albinism Occurrence Congenital false Inferred relationship Some
    Autosomal dominant oculocutaneous albinism Finding site Structure of skin region false Inferred relationship Some 2
    Autosomal dominant oculocutaneous albinism Finding site Eye structure false Inferred relationship Some 1
    Autosomal dominant oculocutaneous albinism Associated morphology congenitale hypopigmentatie false Inferred relationship Some 1
    Autosomal dominant oculocutaneous albinism Finding site Skin structure false Inferred relationship Some 1
    Autosomal dominant oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Some 1
    Autosomal dominant oculocutaneous albinism Finding site Eye structure false Inferred relationship Some 1
    Autosomal dominant oculocutaneous albinism Associated morphology congenitale hypopigmentatie false Inferred relationship Some 1
    Autosomal dominant oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Some 1
    Autosomal dominant oculocutaneous albinism Finding site Skin structure false Inferred relationship Some 1
    Autosomal dominant oculocutaneous albinism Occurrence Congenital false Inferred relationship Some 2
    Autosomal dominant oculocutaneous albinism Associated morphology congenitale hypopigmentatie false Inferred relationship Some 2
    Autosomal dominant oculocutaneous albinism Finding site Skin structure false Inferred relationship Some 2
    Autosomal dominant oculocutaneous albinism Occurrence Congenital false Inferred relationship Some 3
    Autosomal dominant oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Some 3
    Autosomal dominant oculocutaneous albinism Occurrence Congenital false Inferred relationship Some 1
    Autosomal dominant oculocutaneous albinism Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2
    Autosomal dominant oculocutaneous albinism Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Autosomal dominant oculocutaneous albinism Associated morphology Hypopigmentation false Inferred relationship Some 1
    Autosomal dominant oculocutaneous albinism Associated morphology Hypopigmentation false Inferred relationship Some 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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