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52692001: Albinoidism (disorder)

    Status: retired, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    790729018 Albinoidism (disorder) en Fully specified name Active Case insensitive SNOMED CT core
    87685011 Albinoidism en Synonym Active Case insensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Albinoidism Pathological process Pathological developmental process false Inferred relationship Some 1
    Albinoidism Occurrence Congenital false Inferred relationship Some 1
    Albinoidism Associated morphology Hypopigmentation false Inferred relationship Some 1
    Albinoidism Finding site Eye region structure false Inferred relationship Some
    Albinoidism Is a Albinism false Inferred relationship Some
    Albinoidism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
    Albinoidism Finding site Eye structure false Inferred relationship Some 2
    Albinoidism Is a Site-specific disorder of skin false Inferred relationship Some
    Albinoidism Is a Hereditary disorder of the integument false Inferred relationship Some
    Albinoidism Is a Hereditary disorder of the visual system false Inferred relationship Some
    Albinoidism Is a Disorder of tyrosine metabolism false Inferred relationship Some
    Albinoidism Is a Congenital deficiency of pigment of skin false Inferred relationship Some
    Albinoidism Is a Disorder of eye region false Inferred relationship Some
    Albinoidism Associated morphology Decreased melanin pigmentation false Inferred relationship Some
    Albinoidism Finding site Eye region structure false Inferred relationship Some
    Albinoidism Finding site Skin structure false Inferred relationship Some 1
    Albinoidism Finding site Skin structure false Inferred relationship Some 1
    Albinoidism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
    Albinoidism Occurrence Congenital false Inferred relationship Some 2
    Albinoidism Associated morphology Congenital hypopigmentation false Inferred relationship Some 2
    Albinoidism Finding site Skin structure false Inferred relationship Some 2
    Albinoidism Occurrence Congenital false Inferred relationship Some 3
    Albinoidism Associated morphology Decreased melanin pigmentation false Inferred relationship Some 3
    Albinoidism Associated morphology Congenital hypopigmentation false Inferred relationship Some 1
    Albinoidism Finding site Skin structure false Inferred relationship Some 3
    Albinoidism Is a Genetic disorder of skin pigmentation false Inferred relationship Some
    Albinoidism Finding site Eye structure false Inferred relationship Some
    Albinoidism Occurrence Congenital false Inferred relationship Some
    Albinoidism Finding site Structure of skin region false Inferred relationship Some 1
    Albinoidism Associated morphology Congenital deficiency false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Oculocutaneous albinoidism Is a False Albinoidism Inferred relationship Some

    Reference Sets

    Australian dialect reference set

    Concept inactivation indicator reference set

    SAME AS association reference set

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