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773575001: Ocular albinism with congenital sensorineural deafness (disorder)

    Status: retired, Primitive. Date: 31-Oct 2022. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    3724256010 Ocular albinism with congenital sensorineural deafness en Synonym Active Case insensitive SNOMED CT core
    3724257018 Ocular albinism with congenital sensorineural deafness (disorder) en Fully specified name Active Case insensitive SNOMED CT core
    3724258011 Waardenburg syndrome type 2 with ocular albinism en Synonym Active Case sensitive SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Ocular albinism with congenital sensorineural deafness Finding site Structure of auditory system false Inferred relationship Some 1
    Ocular albinism with congenital sensorineural deafness Occurrence Congenital false Inferred relationship Some 3
    Ocular albinism with congenital sensorineural deafness Pathological process Pathological developmental process false Inferred relationship Some 3
    Ocular albinism with congenital sensorineural deafness Is a Ocular albinism false Inferred relationship Some
    Ocular albinism with congenital sensorineural deafness Occurrence Congenital false Inferred relationship Some 2
    Ocular albinism with congenital sensorineural deafness Finding site Skin structure false Inferred relationship Some 2
    Ocular albinism with congenital sensorineural deafness Pathological process Pathological developmental process false Inferred relationship Some 2
    Ocular albinism with congenital sensorineural deafness Occurrence Congenital false Inferred relationship Some 1
    Ocular albinism with congenital sensorineural deafness Is a Genetic disorder of skin pigmentation false Inferred relationship Some
    Ocular albinism with congenital sensorineural deafness Is a Congenital sensorineural hearing loss false Inferred relationship Some
    Ocular albinism with congenital sensorineural deafness Is a Auditory system hereditary disorder false Inferred relationship Some
    Ocular albinism with congenital sensorineural deafness Interprets Hearing false Inferred relationship Some 4
    Ocular albinism with congenital sensorineural deafness Associated morphology Decreased melanin pigmentation false Inferred relationship Some 3
    Ocular albinism with congenital sensorineural deafness Finding site Eye structure false Inferred relationship Some 3
    Ocular albinism with congenital sensorineural deafness Is a Congenital oculocutaneous hypopigmentation false Inferred relationship Some
    Ocular albinism with congenital sensorineural deafness Associated morphology Hypopigmentation false Inferred relationship Some 2
    Ocular albinism with congenital sensorineural deafness Is a Waardenburg syndrome type 2 false Inferred relationship Some
    Ocular albinism with congenital sensorineural deafness Finding site Ear structure false Inferred relationship Some 1
    Ocular albinism with congenital sensorineural deafness Pathological process Pathological developmental process false Inferred relationship Some 1
    Ocular albinism with congenital sensorineural deafness Is a Decreased hearing false Inferred relationship Some
    Ocular albinism with congenital sensorineural deafness Has interpretation Decreased false Inferred relationship Some 4
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Australian emergency department reference set

    Concept inactivation indicator reference set

    REPLACED BY association reference set

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