FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

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) Is a Epidermolysis bullosa simplex true Inferred relationship Some
Autosomal dominant epidermolysis bullosa simplex (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant epidermolysis bullosa simplex (disorder) Associated morphology Epidermolysis true Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Connective tissue structure false Inferred relationship Some
Autosomal dominant epidermolysis bullosa simplex (disorder) Associated morphology Keratolysis false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) Associated morphology Congenital anomaly false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) Associated morphology Blister false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) Occurrence Congenital false Inferred relationship Some
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Skin structure false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Skin structure false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Autosomal dominant epidermolysis bullosa simplex (disorder) Is a Hereditary disorder of the integument false Inferred relationship Some
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Skin structure false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Skin structure false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Skin structure false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Skin structure false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Skin structure false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Skin structure false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Skin structure false Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Skin structure false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Skin structure true Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Skin structure false Inferred relationship Some 2
Autosomal dominant epidermolysis bullosa simplex (disorder) Occurrence Congenital false Inferred relationship Some 3
Autosomal dominant epidermolysis bullosa simplex (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 3
Autosomal dominant epidermolysis bullosa simplex (disorder) Finding site Skin structure false Inferred relationship Some 3
Autosomal dominant epidermolysis bullosa simplex (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal dominant epidermolysis bullosa simplex (disorder) Occurrence Congenital true Inferred relationship Some 1

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

This concept is not in any reference sets

Back to Start