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724206005: Keratin 14 related epidermolysis bullosa simplex (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3432332013 Keratin 14 related epidermolysis bullosa simplex (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3432333015 KRT14 related epidermolysis bullosa simplex en Synonym Active Entire term case sensitive SNOMED CT core module
3432334014 Keratin 14 related epidermolysis bullosa simplex en Synonym Active Entire term case insensitive SNOMED CT core module
3432335010 EBS-AR KRT14 - epidermolysis bullosa simplex autosomal recessive keratin 14 en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Keratin 14 related epidermolysis bullosa simplex Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Keratin 14 related epidermolysis bullosa simplex Is a Basal epidermolysis bullosa simplex true Inferred relationship Existential restriction modifier
Keratin 14 related epidermolysis bullosa simplex Finding site Connective tissue structure false Inferred relationship Existential restriction modifier
Keratin 14 related epidermolysis bullosa simplex Associated morphology Epidermolysis false Inferred relationship Existential restriction modifier 4
Keratin 14 related epidermolysis bullosa simplex Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Keratin 14 related epidermolysis bullosa simplex Finding site Stratum germinativum structure false Inferred relationship Existential restriction modifier 4
Keratin 14 related epidermolysis bullosa simplex Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 5
Keratin 14 related epidermolysis bullosa simplex Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Keratin 14 related epidermolysis bullosa simplex Finding site Skin structure false Inferred relationship Existential restriction modifier 5
Keratin 14 related epidermolysis bullosa simplex Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Keratin 14 related epidermolysis bullosa simplex Finding site Stratum germinativum structure true Inferred relationship Existential restriction modifier 1
Keratin 14 related epidermolysis bullosa simplex Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Keratin 14 related epidermolysis bullosa simplex Associated morphology Epidermolysis true Inferred relationship Existential restriction modifier 1
Keratin 14 related epidermolysis bullosa simplex 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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