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79417003: Autosomal dominant oculocutaneous albinism (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    131767016 Autosomal dominant oculocutaneous albinism en Synonym Active Entire term case insensitive SNOMED CT core module
    820465019 Autosomal dominant oculocutaneous albinism (disorder) 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
    Autosomal dominant oculocutaneous albinism Is a Oculocutaneous albinism false Inferred relationship Existential restriction modifier
    Autosomal dominant oculocutaneous albinism Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
    Autosomal dominant oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 2
    Autosomal dominant oculocutaneous albinism Finding site Skin structure false Inferred relationship Existential restriction modifier 3
    Autosomal dominant oculocutaneous albinism Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
    Autosomal dominant oculocutaneous albinism Occurrence Congenital false Inferred relationship Existential restriction modifier
    Autosomal dominant oculocutaneous albinism Finding site Structure of skin region false Inferred relationship Existential restriction modifier 2
    Autosomal dominant oculocutaneous albinism Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 1
    Autosomal dominant oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
    Autosomal dominant oculocutaneous albinism Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Autosomal dominant oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 1
    Autosomal dominant oculocutaneous albinism Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 1
    Autosomal dominant oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
    Autosomal dominant oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 1
    Autosomal dominant oculocutaneous albinism Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Autosomal dominant oculocutaneous albinism Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Autosomal dominant oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 2
    Autosomal dominant oculocutaneous albinism Finding site Skin structure false Inferred relationship Existential restriction modifier 2
    Autosomal dominant oculocutaneous albinism Occurrence Congenital false Inferred relationship Existential restriction modifier 3
    Autosomal dominant oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 3
    Autosomal dominant oculocutaneous albinism Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Autosomal dominant oculocutaneous albinism Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
    Autosomal dominant oculocutaneous albinism Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Autosomal dominant oculocutaneous albinism Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier 1
    Autosomal dominant oculocutaneous albinism Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier 2
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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