Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1767876017 | Melanocytic neoplasm (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1779238013 | Melanocytic neoplasm | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Melanocytic neoplasm (disorder) | Is a | Neoplastic disease | true | Inferred relationship | Some | ||
| Melanocytic neoplasm (disorder) | Associated morphology | Nevus AND/OR melanoma | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Melanocytic tumor of skin | Is a | True | Melanocytic neoplasm (disorder) | Inferred relationship | Some | |
| Melanoma in situ by body site | Is a | False | Melanocytic neoplasm (disorder) | Inferred relationship | Some | |
| Malignant melanoma (disorder) | Is a | True | Melanocytic neoplasm (disorder) | Inferred relationship | Some | |
| Acquired melanocytic nevus (disorder) | Is a | False | Melanocytic neoplasm (disorder) | Inferred relationship | Some | |
| Melanoma in situ of non-skin site | Is a | False | Melanocytic neoplasm (disorder) | Inferred relationship | Some | |
| Melanocytic nevus (disorder) | Is a | True | Melanocytic neoplasm (disorder) | Inferred relationship | Some | |
| Primary melanocytic lesion of meninges (disorder) | Is a | True | Melanocytic neoplasm (disorder) | Inferred relationship | Some | |
| Melanoma in situ | Is a | True | Melanocytic neoplasm (disorder) | Inferred relationship | Some | |
| Pigmented epithelioid melanocytoma (disorder) | Is a | True | Melanocytic neoplasm (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR