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68897000: Hereditary benign intraepithelial dyskeratosis (disorder)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    114434014 Hereditary benign intraepithelial dyskeratosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    114435010 Witkop's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    114436011 Witkop-Von Sallmann disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    501123018 Witkop's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    501124012 Witkop-Brearley-Gentry syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    501125013 Witkop-von Sallman syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    808782011 Hereditary benign intraepithelial dyskeratosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    114434014 Hereditary benign intraepithelial dyskeratosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    114434014 Hereditary benign intraepithelial dyskeratosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    114435010 Witkop's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    114436011 Witkop-Von Sallmann disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    501123018 Witkop's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    501124012 Witkop-Brearley-Gentry syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    501125013 Witkop-von Sallman syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
    808782011 Hereditary benign intraepithelial dyskeratosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    808782011 Hereditary benign intraepithelial dyskeratosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Hereditary benign intraepithelial dyskeratosis Is a Congenital anomaly of face false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Is a Disorder of oral soft tissues false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Is a Disorder of skin AND/OR subcutaneous tissue of head (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Is a anomalie congénitale de l'appareil respiratoire false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Is a Hereditary disorder of the integument (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Is a Ectodermal dysplasia false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Associated morphology Dyskeratosis false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary benign intraepithelial dyskeratosis Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary benign intraepithelial dyskeratosis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Hereditary benign intraepithelial dyskeratosis Finding site Oral soft tissues structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Finding site Jaw region structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Finding site Oral cavity structure false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier (core metadata concept)
    Hereditary benign intraepithelial dyskeratosis Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

    POSSIBLY EQUIVALENT TO association reference set

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