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725407006: Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type (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
5403458016 A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403459012 A rare dystrophic epidermolysis bullosa (DEB) characterised by generalised cutaneous and mucosal blistering that is not associated with severe deformities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3442281010 Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3442282015 Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3442283013 RDEB-O - recessive dystrophic epidermolysis bullosa-generalized other en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3442284019 RDEB-O - recessive dystrophic epidermolysis bullosa-generalised other en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
7615761000241115 EBDR (épidermolyse bulleuse dystrophique récessive) de type non Hallopeau-Siemens fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7615771000241111 épidermolyse bulleuse dystrophique récessive de type non Hallopeau-Siemens fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3447511001000114 Epidermolysis bullosa, dystrophe, generalisierte, autosomal-rezessive, intermediäre Form de 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
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. Is a Recessive dystrophic epidermolysis bullosa true Inferred relationship Some
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. Is a Generalized dystrophic epidermolysis bullosa true Inferred relationship Some
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. Finding site Connective tissue structure false Inferred relationship Some
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. Associated morphology Epidermolysis false Inferred relationship Some 4
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. Occurrence Congenital false Inferred relationship Some 4
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. Finding site Skin structure false Inferred relationship Some 4
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. Associated morphology anomalie du développement false Inferred relationship Some 5
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. Occurrence Congenital false Inferred relationship Some 5
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. Finding site Skin structure false Inferred relationship Some 5
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. Finding site Skin structure true Inferred relationship Some 1
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. Associated morphology Epidermolysis true Inferred relationship Some 1
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. Occurrence Congenital true Inferred relationship Some 1
A rare dystrophic epidermolysis bullosa (DEB) characterized by generalized cutaneous and mucosal blistering that is not associated with severe deformities. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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