Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3643759018 | Erythema palmare hereditarium | en | Synonym | Active | Case insensitive | SNOMED CT core |
3643760011 | Erythema palmare hereditarium (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3643761010 | Red palms disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
3643762015 | Lane disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
3643763013 | A rare benign congenital genetic skin disorder with characteristics of permanent and asymptomatic erythema of the palmar and less frequently the solar surfaces. In most cases, it presents with sharply demarcated redness of the thenar and hypothenar eminences, as well as the palmar aspect of the phalanges, with scattered telangiectasia spots that do not cause any discomfort (pain, itching or burning) to the patient. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Erythema palmare hereditarium | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Erythema palmare hereditarium | Is a | Palmar erythema | true | Inferred relationship | Some | ||
Erythema palmare hereditarium | Is a | Congenital disease | true | Inferred relationship | Some | ||
Erythema palmare hereditarium | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
Erythema palmare hereditarium | Associated morphology | Erythema | true | Inferred relationship | Some | 1 | |
Erythema palmare hereditarium | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Erythema palmare hereditarium | Finding site | Skin structure of palmar area of hand | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set