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398170002: Autosomal dominant epidermolysis bullosa simplex (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1766089015 Autosomal dominant epidermolysis bullosa simplex (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1777726013 Autosomal dominant epidermolysis bullosa simplex en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786149016 EBS 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant epidermolysis bullosa simplex (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) est un(e) (attribut) Epidermolysis bullosa simplex true Inferred relationship Some
Autosomal dominant epidermolysis bullosa simplex (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant epidermolysis bullosa simplex (disorder) morphologie associée (attribut) Epidermolysis true Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) Connective tissue structure false Inferred relationship Some
Autosomal dominant epidermolysis bullosa simplex (disorder) morphologie associée (attribut) Keratolysis false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) morphologie associée (attribut) Blister false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) survenue (attribut) congénital false Inferred relationship Some
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) est un(e) (attribut) Connective tissue hereditary disorder false Inferred relationship Some
Autosomal dominant epidermolysis bullosa simplex (disorder) est un(e) (attribut) Hereditary disorder of the integument false Inferred relationship Some
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) survenue (attribut) congénital false Inferred relationship Some 3
Autosomal dominant epidermolysis bullosa simplex (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 3
Autosomal dominant epidermolysis bullosa simplex (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Weber-Cockayne syndrome est un(e) (attribut) True Autosomal dominant epidermolysis bullosa simplex (disorder) Inferred relationship Some
Intermediate epidermolysis bullosa simplex with cardiomyopathy (disorder) est un(e) (attribut) True Autosomal dominant epidermolysis bullosa simplex (disorder) Inferred relationship Some
Epidermolysis bullosa simplex, Ogna type (disorder) est un(e) (attribut) True Autosomal dominant epidermolysis bullosa simplex (disorder) Inferred relationship Some
Epidermolysis bullosa simplex with circinate migratory erythema (disorder) est un(e) (attribut) True Autosomal dominant epidermolysis bullosa simplex (disorder) Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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