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 |
5401499019 | A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401500011 | A rare hereditary skin disease characterised by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308619016 | Punctate palmoplantar keratoderma type 1 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3308620010 | Punctate palmoplantar keratoderma type 1 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3308621014 | Buschke Fischer Brauer syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3308622019 | Keratodermia palmoplantaris papulosa Buschke Fischer Brauer type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
927921000172118 | kératodermie palmoplantaire ponctuée type 1 | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
1014201000172114 | KPPP1 - kératodermie palmoplantaire ponctuée type 1 | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3409031001000110 | Palmoplantarkeratose, punktierte, Typ I | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Is a | Autosomal dominant hereditary disorder (disorder) | true | Inferred relationship | Some | ||
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Is a | Punctate palmoplantar keratoderma (disorder) | true | Inferred relationship | Some | ||
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Has definitional manifestation | Abnormal keratinization | false | Inferred relationship | Some | ||
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Finding site | Skin structure | false | Inferred relationship | Some | 3 | |
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Finding site | Skin structure | false | Inferred relationship | Some | 4 | |
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Associated morphology | anomalie du développement | false | Inferred relationship | Some | 3 | |
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Associated morphology | Hyperkeratosis | false | Inferred relationship | Some | 4 | |
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Has interpretation | Abnormal | false | Inferred relationship | Some | 1 | |
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Interprets | Keratinization | false | Inferred relationship | Some | 1 | |
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 2 | |
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Finding site | Skin structure of palmar area of hand | true | Inferred relationship | Some | 2 | |
A rare hereditary skin disease characterized by irregularly distributed epidermal papular/punctate hyperkeratosis of the palms and soles with wide variation among patients. | Finding site | Skin structure of sole of foot | 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)