Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
132485010 | Congenital junctional epidermolysis bullosa | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
132486011 | Epidermolysis bullosa, junctional Herlitz-Pearson type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
132487019 | Epidermolysis bullosa hereditaria letalis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
820951013 | Congenital junctional epidermolysis bullosa (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
998161000241111 | épidermolyse bulleuse jonctionnelle congénitale | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital junctional epidermolysis bullosa-pyloric atresia syndrome | Is a | True | Congenital junctional epidermolysis bullosa | Inferred relationship | Some | |
LOC syndrome is a subtype of junctional epidermolysis bullosa characterized by an altered cry in the neonatal period and by aberrant production of granulation tissue in particular affecting the upper airway tract, conjunctiva and periungual/subungual sites. | Is a | True | Congenital junctional epidermolysis bullosa | Inferred relationship | Some |
This concept is not in any reference sets