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723163000: epidermolyse bulleuse simple basale (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3334762019 Basal epidermolysis bullosa simplex (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334763012 Basal epidermolysis bullosa simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
759001000241116 epidermolyse bulleuse simple basale (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
947781000172119 epidermolyse bulleuse simple basale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Basal epidermolysis bullosa simplex (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Basal epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) Stratum germinativum true Inferred relationship Some 1
Basal epidermolysis bullosa simplex (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Basal epidermolysis bullosa simplex (disorder) morphologie associée (attribut) Epidermolysis true Inferred relationship Some 1
Basal epidermolysis bullosa simplex (disorder) est un(e) (attribut) Epidermolysis bullosa simplex true Inferred relationship Some
Basal epidermolysis bullosa simplex (disorder) est un(e) (attribut) Connective tissue hereditary disorder false Inferred relationship Some
Basal epidermolysis bullosa simplex (disorder) est un(e) (attribut) Hereditary disorder of the integument false Inferred relationship Some
Basal epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) Connective tissue structure false Inferred relationship Some
Basal epidermolysis bullosa simplex (disorder) morphologie associée (attribut) Epidermolysis false Inferred relationship Some 4
Basal epidermolysis bullosa simplex (disorder) survenue (attribut) congénital false Inferred relationship Some 4
Basal epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) Stratum germinativum false Inferred relationship Some 4
Basal epidermolysis bullosa simplex (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 5
Basal epidermolysis bullosa simplex (disorder) survenue (attribut) congénital false Inferred relationship Some 5
Basal epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 5

Inbound Relationships Type Active Source Characteristic Refinability Group
Epidermolysis bullosa simplex with muscular dystrophy (disorder) est un(e) (attribut) True Basal epidermolysis bullosa simplex (disorder) Inferred relationship Some
Keratin 14 related epidermolysis bullosa simplex (disorder) est un(e) (attribut) True Basal epidermolysis bullosa simplex (disorder) Inferred relationship Some

This concept is not in any reference sets

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