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


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

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 (core metadata concept) SNOMED CT core
3723744017 Epidermolysis bullosa simplex due to BP230 deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3723747012 DST (dystonin) related epidermolysis bullosa simplex en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3723742018 A rare hereditary basal epidermolysis bullosa simplex characterized by mild, predominantly acral, trauma-induced skin fragility, resulting in blisters. Blisters mostly affect the feet, including the dorsal side, and are often several centimeters big. There is evidence the disease is caused by homozygous mutation in the DST (BPAG1) gene on chromosome 6p12. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3723745016 A rare hereditary basal epidermolysis bullosa simplex characterised by mild, predominantly acral, trauma-induced skin fragility, resulting in blisters. Blisters mostly affect the feet, including the dorsal side, and are often several centimetres big. There is evidence the disease is caused by homozygous mutation in the DST (BPAG1) gene on chromosome 6p12. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4208751000052115 epidermolysis bullosa simplex orsakad av BP230-brist sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) Finding site Connective tissue structure false Inferred relationship Some
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) Is a Epidermolysis bullosa simplex false Inferred relationship Some
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) Is a Autosomal recessive hereditary disorder false Inferred relationship Some
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) Associated morphology Epidermolysis true Inferred relationship Some 1
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) Is a Hereditary disorder of the integument false Inferred relationship Some
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) Finding site Skin structure true Inferred relationship Some 1
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) Occurrence Congenital true Inferred relationship Some 1
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) Is a Autosomal recessive epidermolysis bullosa simplex true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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