Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
358288014 | Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
358289018 | Polykeratosis of Touraine | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
628046019 | Papuloverrucous palmoplantar keratoderma of Jakac-Wolf (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 2 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Finding site | Skin structure of palmar area of hand | true | Inferred relationship | Some | 2 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Finding site | Skin structure of sole of foot | true | Inferred relationship | Some | 1 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Associated morphology | Hyperkeratosis | false | Inferred relationship | Some | 1 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Has definitional manifestation | Abnormal keratinisation | false | Inferred relationship | Some | ||
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 1 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Associated morphology | Hyperkeratosis | false | Inferred relationship | Some | 4 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Is a | Hereditary palmoplantar keratoderma | true | Inferred relationship | Some | ||
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 1 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 2 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Finding site | Skin structure of palmar area of hand | false | Inferred relationship | Some | 3 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Finding site | Skin structure of sole of foot | false | Inferred relationship | Some | 4 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Occurrence | Congenital | false | Inferred relationship | Some | ||
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Is a | Circumscribed palmoplantar keratoderma | false | Inferred relationship | Some | ||
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Has interpretation | Abnormal | false | Inferred relationship | Some | 2 | |
Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Interprets | Keratinisation | false | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set