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

20512000: Dominant congenital ichthyosiform erythroderma (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2015. Module: SNOMED CT core module

    Descriptions:

    Id Description Lang Type Status Case? Module
    34515018 Dominant congenital ichthyosiform erythroderma en Synonym Active Entire term case insensitive SNOMED CT core module
    34516017 Dominant ichthyosis vulgaris en Synonym Active Entire term case insensitive SNOMED CT core module
    34517014 Epidermolytic hyperkeratosis en Synonym Active Entire term case insensitive SNOMED CT core module
    34518016 Congenital bullous ichthyosiform erythroderma en Synonym Active Entire term case insensitive SNOMED CT core module
    749681018 Dominant congenital ichthyosiform erythroderma (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
    Dominant congenital ichthyosiform erythroderma Is a Congenital ichthyosis of skin false Inferred relationship Existential restriction modifier
    Dominant congenital ichthyosiform erythroderma Finding site Structure of skin region false Inferred relationship Existential restriction modifier
    Dominant congenital ichthyosiform erythroderma Occurrence Congenital false Inferred relationship Existential restriction modifier
    Dominant congenital ichthyosiform erythroderma Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Dominant congenital ichthyosiform erythroderma Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Dominant congenital ichthyosiform erythroderma Finding site Skin structure false Inferred relationship Existential restriction modifier 1
    Dominant congenital ichthyosiform erythroderma Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
    Dominant congenital ichthyosiform erythroderma Occurrence Congenital false Inferred relationship Existential restriction modifier 2
    Dominant congenital ichthyosiform erythroderma Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
    Dominant congenital ichthyosiform erythroderma Finding site Skin structure false Inferred relationship Existential restriction modifier 2

    Inbound Relationships Type Active Source Characteristic Refinability Group

    This concept is not in any reference sets

    Back to Start