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68897000: Hereditary benign intraepithelial dyskeratosis (disorder)

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

    Descriptions:

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

    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
    Hereditary benign intraepithelial dyskeratosis Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier
    Hereditary benign intraepithelial dyskeratosis Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
    Hereditary benign intraepithelial dyskeratosis Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier
    Hereditary benign intraepithelial dyskeratosis Is a Disorder of oral soft tissues false Inferred relationship Existential restriction modifier
    Hereditary benign intraepithelial dyskeratosis Is a Disorder of skin AND/OR subcutaneous tissue of head false Inferred relationship Existential restriction modifier
    Hereditary benign intraepithelial dyskeratosis Is a Congenital anomaly of respiratory system false Inferred relationship Existential restriction modifier
    Hereditary benign intraepithelial dyskeratosis Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
    Hereditary benign intraepithelial dyskeratosis Is a Ectodermal dysplasia false Inferred relationship Existential restriction modifier
    Hereditary benign intraepithelial dyskeratosis Associated morphology Dyskeratosis false Inferred relationship Existential restriction modifier 1
    Hereditary benign intraepithelial dyskeratosis Associated morphology Dysplasia false Inferred relationship Existential restriction modifier 1
    Hereditary benign intraepithelial dyskeratosis Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Hereditary benign intraepithelial dyskeratosis Finding site Oral soft tissues structure false Inferred relationship Existential restriction modifier
    Hereditary benign intraepithelial dyskeratosis Finding site Jaw region structure false Inferred relationship Existential restriction modifier
    Hereditary benign intraepithelial dyskeratosis Occurrence Congenital false Inferred relationship Existential restriction modifier
    Hereditary benign intraepithelial dyskeratosis Finding site Oral cavity structure false Inferred relationship Existential restriction modifier
    Hereditary benign intraepithelial dyskeratosis Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier
    Hereditary benign intraepithelial dyskeratosis Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

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