Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3304749017 | Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3304750017 | Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3304751018 | Non-epidermolytic palmoplantar keratoderma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
6328281000146113 | niet-epidermolytische palmoplantaire keratodermie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
6328311000146111 | niet-epidermolytische keratosis palmoplantaris | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
12689201000146110 | autosomaal dominante diffuse palmoplantaire keratoderma Norrbotten-type (aandoening) | nl | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
12740691000146110 | autosomaal dominante diffuse palmoplantaire keratoderma Norrbotten-type | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
3304752013 | This syndrome has manifestation of a diffuse non-epidermolytic palmoplantar keratoderma with frequent fungal infections. Prevalence in the general population is estimated at 1 in 40,000 but is much higher in northern Sweden. Transmission is autosomal dominant and the causative gene has been localised to chromosome 12q11-q13. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3304802010 | This syndrome has manifestation of a diffuse non-epidermolytic palmoplantar keratoderma with frequent fungal infections. Prevalence in the general population is estimated at 1 in 40,000 but is much higher in northern Sweden. Transmission is autosomal dominant and the causative gene has been localized to chromosome 12q11-q13. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Is a | Hereditary diffuse palmoplantar keratoderma (disorder) | true | Inferred relationship | Some | ||
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Has definitional manifestation | Abnormal keratinization | false | Inferred relationship | Some | ||
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 3 | |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 4 | |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Associated morphology | gebrekkige ontwikkeling (afwijkende morfologie) | false | Inferred relationship | Some | 3 | |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Associated morphology | Hyperkeratosis | false | Inferred relationship | Some | 4 | |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Has interpretation | Abnormal | false | Inferred relationship | Some | 1 | |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Interprets | Keratinization | false | Inferred relationship | Some | 1 | |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Finding site | Skin structure of sole of foot (body structure) | false | Inferred relationship | Some | 1 | |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Finding site | Skin structure of palmar area of hand | false | Inferred relationship | Some | 2 | |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 2 | |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Finding site | Entire skin of palmar area of hand | true | Inferred relationship | Some | 1 | |
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type (disorder) | Finding site | Entire skin of sole of foot | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set