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716699004: Epidermolysis bullosa simplex due to plakophilin deficiency (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
3307241013 Epidermolysis bullosa simplex due to plakophilin deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3307242018 Epidermolysis bullosa simplex due to plakophilin deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
3307243011 McGrath syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3307244017 Ectodermal dysplasia skin fragility syndrome 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
Epidermolysis bullosa simplex due to plakophilin deficiency Is a Epidermolysis bullosa simplex false Inferred relationship Existential restriction modifier
Epidermolysis bullosa simplex due to plakophilin deficiency Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Epidermolysis bullosa simplex due to plakophilin deficiency Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Epidermolysis bullosa simplex due to plakophilin deficiency Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Epidermolysis bullosa simplex due to plakophilin deficiency Finding site Connective tissue structure false Inferred relationship Existential restriction modifier
Epidermolysis bullosa simplex due to plakophilin deficiency Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Epidermolysis bullosa simplex due to plakophilin deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Epidermolysis bullosa simplex due to plakophilin deficiency Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Epidermolysis bullosa simplex due to plakophilin deficiency Associated morphology Epidermolysis false Inferred relationship Existential restriction modifier 4
Epidermolysis bullosa simplex due to plakophilin deficiency Finding site Skin structure false Inferred relationship Existential restriction modifier 4
Epidermolysis bullosa simplex due to plakophilin deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa simplex due to plakophilin deficiency Associated morphology Epidermolysis true Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa simplex due to plakophilin deficiency Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa simplex due to plakophilin deficiency Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa simplex due to plakophilin deficiency Is a Autosomal recessive epidermolysis bullosa simplex true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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