Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5402851012 | A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5429767019 | A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterised by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3331144018 | Palmoplantar keratoderma Nagashima type (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3331145017 | Palmoplantar keratoderma Nagashima type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
903381000172117 | hyperkératose palmoplantaire type Nagashima | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
994751000172111 | kératodermie palmoplantaire type Nagashima | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3432231001000115 | Palmoplantarkeratose Typ Nagashima | 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 autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Is a | Hereditary diffuse palmoplantar keratoderma (disorder) | true | Inferred relationship | Some | ||
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Has definitional manifestation | Abnormal keratinization | false | Inferred relationship | Some | ||
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Associated morphology | Hyperkeratosis | false | Inferred relationship | Some | 3 | |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Finding site | Skin structure | false | Inferred relationship | Some | 3 | |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Associated morphology | anomalie du développement | false | Inferred relationship | Some | 4 | |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Finding site | Skin structure | false | Inferred relationship | Some | 4 | |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Is a | Congenital disease | false | Inferred relationship | Some | ||
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Interprets | Keratinization | false | Inferred relationship | Some | 2 | |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Has interpretation | Abnormal | false | Inferred relationship | Some | 2 | |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 2 | |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Finding site | Skin structure of palmar area of hand | false | Inferred relationship | Some | 1 | |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Finding site | Skin structure of sole of foot | false | Inferred relationship | Some | 2 | |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Finding site | Entire skin of sole of foot | true | Inferred relationship | Some | 1 | |
A rare autosomal recessive, isolated diffuse palmoplantar keratoderma characterized by transgressive and nonprogressive palmoplantar keratoderma resembling a mild form of mal de Meleda. | Finding site | Entire skin of palmar area of hand (body structure) | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)