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11243003: Oculocutaneous albinoidism (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
    19473012 Oculocutaneous albinoidism en Synonym Active Entire term case insensitive SNOMED CT core module
    640064017 Oculocutaneous albinoidism (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
    Oculocutaneous albinoidism Is a Albinoidism false Inferred relationship Existential restriction modifier
    Oculocutaneous albinoidism Finding site Structure of eye proper false Inferred relationship Existential restriction modifier
    Oculocutaneous albinoidism Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
    Oculocutaneous albinoidism Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
    Oculocutaneous albinoidism Occurrence Congenital false Inferred relationship Existential restriction modifier
    Oculocutaneous albinoidism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
    Oculocutaneous albinoidism Finding site Skin structure false Inferred relationship Existential restriction modifier 3
    Oculocutaneous albinoidism Finding site Eye region structure false Inferred relationship Existential restriction modifier
    Oculocutaneous albinoidism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 2
    Oculocutaneous albinoidism Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 2
    Oculocutaneous albinoidism Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier
    Oculocutaneous albinoidism Finding site Eye region structure false Inferred relationship Existential restriction modifier
    Oculocutaneous albinoidism Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Oculocutaneous albinoidism Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Oculocutaneous albinoidism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
    Oculocutaneous albinoidism Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Oculocutaneous albinoidism Occurrence Congenital false Inferred relationship Existential restriction modifier 3
    Oculocutaneous albinoidism Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 2
    Oculocutaneous albinoidism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 3
    Oculocutaneous albinoidism Finding site Skin structure false Inferred relationship Existential restriction modifier 3
    Oculocutaneous albinoidism Occurrence Congenital false Inferred relationship Existential restriction modifier 1
    Oculocutaneous albinoidism Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
    Oculocutaneous albinoidism Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Punctate oculocutaneous albinoidism Is a False Oculocutaneous albinoidism Inferred relationship Existential restriction modifier

    This concept is not in any reference sets

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