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 |
| 175960014 | Howel-Evans' syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 202934012 | Diffuse palmoplantar keratoderma with esophageal cancer | en | Synonym (core metadata concept) | Inactive | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 357696011 | Howel-Evans-Clark syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 357697019 | Keratoderma with carcinoma of oesophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 357698012 | Diffuse palmoplantar keratoderma with oesophageal cancer | en | Synonym (core metadata concept) | Inactive | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 357699016 | Keratoderma with carcinoma of esophagus | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 627560010 | Howel-Evans' syndrome (disorder) | en | Fully specified name | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3036100017 | Howel Evans syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5444510018 | Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5444511019 | Bennion Patterson syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5444512014 | Palmoplantar keratoderma oesophageal carcinoma syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5444513016 | Palmoplantar keratoderma esophageal carcinoma syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5444514010 | Tylosis oesophageal carcinoma syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5444515011 | Tylosis esophageal carcinoma syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5444518013 | Keratosis palmoplantaris esophageal carcinoma syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5444519017 | Keratosis palmoplantaris oesophageal carcinoma syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5444520011 | Palmoplantar hyperkeratosis esophageal carcinoma syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5444521010 | Palmoplantar hyperkeratosis oesophageal carcinoma syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2884620010 | A form of diffuse palmoplantar keratoderma that occurs between the ages of 5 and 15 and may be associated with the subsequent development of esophageal cancer | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3777447014 | A form of diffuse palmoplantar keratoderma that occurs between the ages of 5 and 15 and may be associated with the subsequent development of esophageal cancer. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3777448016 | A form of diffuse palmoplantar keratoderma that occurs between the ages of 5 and 15 and may be associated with the subsequent development of oesophageal cancer. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5444516012 | A rare genetic disease characterised by thickening of the skin on palms and soles restricted to areas of weight bearing and/or friction (focal, non-epidermolytic palmoplantar keratoderma) and oral and oesophageal leucokeratosis, associated with a very high lifetime risk of developing squamous cell carcinoma of the oesophagus. The skin lesions appear in childhood and can be complicated by fissuring and infection. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5444517015 | A rare genetic disease characterized by thickening of the skin on palms and soles restricted to areas of weight bearing and/or friction (focal, non-epidermolytic palmoplantar keratoderma) and oral and esophageal leukokeratosis, associated with a very high lifetime risk of developing squamous cell carcinoma of the esophagus. The skin lesions appear in childhood and can be complicated by fissuring and infection. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Is a | Circumscribed palmoplantar keratoderma | true | Inferred relationship | Some | ||
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Is a | Diffuse palmoplantar keratoderma | false | Inferred relationship | Some | ||
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Finding site | Skin structure of sole of foot (body structure) | true | Inferred relationship | Some | 1 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Finding site | Skin structure of palmar area of hand | false | Inferred relationship | Some | 1 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Associated morphology | Hyperkeratosis | false | Inferred relationship | Some | 1 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 1 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Has definitional manifestation | Abnormal keratinization | false | Inferred relationship | Some | ||
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Is a | Hereditary palmoplantar keratoderma | false | Inferred relationship | Some | ||
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Is a | Carcinoma of esophagus (disorder) | false | Inferred relationship | Some | ||
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Associated morphology | Carcinoma, no subtype | false | Inferred relationship | Some | 2 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Finding site | Oesophageal structure | false | Inferred relationship | Some | 2 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | 1 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 2 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Has interpretation | Abnormal | false | Inferred relationship | Some | 2 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Interprets | Keratinization | false | Inferred relationship | Some | 2 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Finding site | Skin structure of palmar area of hand | true | Inferred relationship | Some | 2 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Associated morphology | Hyperkeratosis | false | Inferred relationship | Some | 2 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Associated morphology | Focal hyperkeratosis | true | Inferred relationship | Some | 2 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Associated morphology | Focal hyperkeratosis | true | Inferred relationship | Some | 1 | |
| Palmoplantar keratoderma esophageal carcinoma syndrome (disorder) | Is a | Hereditary cancer-predisposing syndrome | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR