FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

773575001: oculocutaan albinisme met congenitaal perceptief gehoorverlies (aandoening)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3724257018 Ocular albinism with congenital sensorineural deafness (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3724258011 Waardenburg syndrome type 2 with ocular albinism en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    6485551000146110 oculocutaan albinisme met congenitaal perceptief gehoorverlies nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    6485561000146113 syndroom van Waardenburg type 2 met oculair albinisme nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    6485571000146119 oculocutaan albinisme met congenitaal perceptief gehoorverlies (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

    0 descendants.

    Expanded Value Set

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

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

    Back to Start