FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

52692001: Albinoidism (disorder)

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

    Descriptions:

    Id Description Lang Type Status Case? Module
    87685011 Albinoidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    790729018 Albinoidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    50008271000188111 albinoïdisme fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

    0 descendants.

    Expanded Value Set

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

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    US English

    SAME AS association reference set (foundation metadata concept)

    Back to Start