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716699004: Epidermolysis bullosa simplex due to plakophilin deficiency (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3307241013 Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307242018 Epidermolysis bullosa simplex due to plakophilin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3307243011 McGrath syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3307244017 Ectodermal dysplasia skin fragility syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401370011 Epidermolysis bullosa simplex due to plakophilin deficiency (EBS-PD) is a suprabasal subtype of epidermolysis bullosa simplex characterized by generalized superficial erosions and less commonly blistering. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401371010 Epidermolysis bullosa simplex due to plakophilin deficiency (EBS-PD) is a suprabasal subtype of epidermolysis bullosa simplex characterised by generalised superficial erosions and less commonly blistering. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Is a Epidermolysis bullosa simplex false Inferred relationship Some
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Is a Hereditary disorder of the integument false Inferred relationship Some
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Finding site Connective tissue structure false Inferred relationship Some
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 3
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Occurrence Congenital false Inferred relationship Some 3
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Finding site Skin structure false Inferred relationship Some 3
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Associated morphology Epidermolysis false Inferred relationship Some 4
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Finding site Skin structure false Inferred relationship Some 4
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Occurrence Congenital true Inferred relationship Some 1
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Associated morphology Epidermolysis true Inferred relationship Some 1
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Finding site Skin structure true Inferred relationship Some 1
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) Is a Autosomal recessive epidermolysis bullosa simplex true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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