Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3768166017 | Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3768167014 | Palmoplantar keratoderma, spastic paralysis syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3768168016 | Powell Venencie Gordon syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3768169012 | A rare genetic punctate palmoplantar keratoderma disease with characteristics of discrete focal punctate keratoderma on the palms and soles and/or slowly progressive spastic paralysis, predominantly affecting the lower limbs. Lesional histology reveals pronounced orthokeratosis, acanthosis, papillomatosis, and regular undulation to the surface keratin. There have been no further descriptions in the literature since 1983. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4343241000052118 | syndrom med palmoplantar keratodermi och spastisk pares | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | Interprets | Keratinization | true | Inferred relationship | Some | 2 | |
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | Is a | Punctate palmoplantar keratoderma (disorder) | true | Inferred relationship | Some | ||
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | Is a | Inherited disorder of keratinisation | true | Inferred relationship | Some | ||
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | Finding site | Skin structure of sole of foot (body structure) | true | Inferred relationship | Some | 1 | |
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 3 | |
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | Is a | Keratosis | false | Inferred relationship | Some | ||
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | Finding site | Skin structure of palmar area of hand | true | Inferred relationship | Some | 3 | |
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | Is a | Rough skin (finding) | false | Inferred relationship | Some | ||
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) | Is a | Rough skin of hands | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set