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725419003: Centripetalis recessive dystrophic epidermolysis bullosa (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3442495011 Centripetalis recessive dystrophic epidermolysis bullosa (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3442496012 Centripetalis recessive dystrophic epidermolysis bullosa en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3442497015 Centripetal recessive dystrophic epidermolysis bullosa en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3442498013 RDEB-Ce - recessive dystrophic epidermolysis bullosa centripetalis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3442495011 Centripetalis recessive dystrophic epidermolysis bullosa (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3442496012 Centripetalis recessive dystrophic epidermolysis bullosa en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3442497015 Centripetal recessive dystrophic epidermolysis bullosa en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3442498013 RDEB-Ce - recessive dystrophic epidermolysis bullosa centripetalis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3442499017 An extremely rare subtype of dystrophic epidermolysis bullosa with characteristics of blistering, which begins acrally and then progressively, spreads toward the trunk. Less than ten cases have been reported to date. Onset is usually at birth or during infancy. The centripetal progression of blister formation is slow and occurs over decades. Healing of blisters is associated with milia formation, atrophic scarring and nail dystrophy. Mucosal involvement is usually absent. The disease is caused by mutations within the type VII collagen gene (COL7A1). Mutations in this gene lead to an alteration in function or to a reduction in the amounts of collagen VII. This impairs its assembly into anchoring fibrils that anchor the basement membrane to the underlying dermis. The disease follows an autosomal recessive pattern of inheritance. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
873071000172117 epidermolyse bulleuse dystrophique récessive centripète fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
940441000172117 EBDR (epidermolyse bulleuse dystrophique récessive) centripète fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
873071000172117 epidermolyse bulleuse dystrophique récessive centripète fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
940441000172117 EBDR (epidermolyse bulleuse dystrophique récessive) centripète fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Centripetalis recessive dystrophic epidermolysis bullosa Is a Recessive dystrophic epidermolysis bullosa true Inferred relationship Existential restriction modifier (core metadata concept)
Centripetalis recessive dystrophic epidermolysis bullosa Finding site Connective tissue structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Centripetalis recessive dystrophic epidermolysis bullosa Associated morphology Epidermolysis (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 4
Centripetalis recessive dystrophic epidermolysis bullosa Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Centripetalis recessive dystrophic epidermolysis bullosa Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Centripetalis recessive dystrophic epidermolysis bullosa Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 5
Centripetalis recessive dystrophic epidermolysis bullosa Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
Centripetalis recessive dystrophic epidermolysis bullosa Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 5
Centripetalis recessive dystrophic epidermolysis bullosa Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Centripetalis recessive dystrophic epidermolysis bullosa Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Centripetalis recessive dystrophic epidermolysis bullosa Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Centripetalis recessive dystrophic epidermolysis bullosa Associated morphology Epidermolysis (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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