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239071005: Epidermolytic palmoplantar keratoderma of Vorner (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
358275011 Epidermolytic palmoplantar keratoderma of Vorner en Synonym Active Only initial character case insensitive SNOMED CT core module
358276012 Epidermolytic palmoplantar hyperkeratosis en Synonym Active Entire term case insensitive SNOMED CT core module
628038015 Epidermolytic palmoplantar keratoderma of Vorner (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Epidermolytic palmoplantar keratoderma of Vorner Is a Hereditary palmoplantar keratoderma false Inferred relationship Existential restriction modifier
Epidermolytic palmoplantar keratoderma of Vorner Occurrence Congenital false Inferred relationship Existential restriction modifier
Epidermolytic palmoplantar keratoderma of Vorner Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Epidermolytic palmoplantar keratoderma of Vorner Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Epidermolytic palmoplantar keratoderma of Vorner Has definitional manifestation Abnormal keratinization false Inferred relationship Existential restriction modifier
Epidermolytic palmoplantar keratoderma of Vorner Is a Hereditary diffuse palmoplantar keratoderma true Inferred relationship Existential restriction modifier
Epidermolytic palmoplantar keratoderma of Vorner Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Epidermolytic palmoplantar keratoderma of Vorner Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Epidermolytic palmoplantar keratoderma of Vorner Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Epidermolytic palmoplantar keratoderma of Vorner Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Epidermolytic palmoplantar keratoderma of Vorner Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Epidermolytic palmoplantar keratoderma of Vorner Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 1
Epidermolytic palmoplantar keratoderma of Vorner Has interpretation Abnormal false Inferred relationship Existential restriction modifier 2
Epidermolytic palmoplantar keratoderma of Vorner Interprets Keratinization, function false Inferred relationship Existential restriction modifier 2
Epidermolytic palmoplantar keratoderma of Vorner Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 2
Epidermolytic palmoplantar keratoderma of Vorner Finding site Skin structure of palmar area of hand false Inferred relationship Existential restriction modifier 2
Epidermolytic palmoplantar keratoderma of Vorner Finding site Skin structure of sole of foot false Inferred relationship Existential restriction modifier 1
Epidermolytic palmoplantar keratoderma of Vorner Finding site Entire skin of palmar area of hand true Inferred relationship Existential restriction modifier 1
Epidermolytic palmoplantar keratoderma of Vorner Finding site Entire skin of sole of foot true Inferred relationship Existential restriction modifier 2
Epidermolytic palmoplantar keratoderma of Vorner Is a Autosomal dominant hereditary disorder true 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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