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773501006: Epidermolysis bullosa simplex due to BP230 deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3723743011 Epidermolysis bullosa simplex due to BP230 deficiency (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3723744017 Epidermolysis bullosa simplex due to BP230 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
3723747012 DST (dystonin) related epidermolysis bullosa simplex 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
Epidermolysis bullosa simplex due to BP230 deficiency Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Epidermolysis bullosa simplex due to BP230 deficiency Finding site Connective tissue structure false Inferred relationship Existential restriction modifier
Epidermolysis bullosa simplex due to BP230 deficiency Is a Epidermolysis bullosa simplex false Inferred relationship Existential restriction modifier
Epidermolysis bullosa simplex due to BP230 deficiency Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Epidermolysis bullosa simplex due to BP230 deficiency Associated morphology Epidermolysis true Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa simplex due to BP230 deficiency Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Epidermolysis bullosa simplex due to BP230 deficiency Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa simplex due to BP230 deficiency Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa simplex due to BP230 deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Epidermolysis bullosa simplex due to BP230 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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