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716105001: Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3304749017 Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3304750017 Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type en Synonym Active Only initial character case insensitive SNOMED CT core module
3304751018 Non-epidermolytic palmoplantar keratoderma en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Is a Hereditary diffuse palmoplantar keratoderma true Inferred relationship Existential restriction modifier
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Has definitional manifestation Abnormal keratinization false Inferred relationship Existential restriction modifier
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Finding site Skin structure false Inferred relationship Existential restriction modifier 4
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Associated morphology Hyperkeratosis false Inferred relationship Existential restriction modifier 4
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Has interpretation Abnormal false Inferred relationship Existential restriction modifier 1
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Interprets Keratinization, function false Inferred relationship Existential restriction modifier 1
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Finding site Skin structure of sole of foot false Inferred relationship Existential restriction modifier 1
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 1
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Finding site Skin structure of palmar area of hand false Inferred relationship Existential restriction modifier 2
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 2
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Finding site Entire skin of palmar area of hand true Inferred relationship Existential restriction modifier 1
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type Finding site Entire skin of sole of foot true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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