Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5066124018 | Combined hamartoma of retina and retinal pigment epithelium | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5066125017 | CHR-RPE - combined hamartoma of retina and retinal pigment epithelium | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5066126016 | Combined hamartoma of retina and retinal pigment epithelium (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5066127013 | A rare benign eye tumor characterized by the presence of glial cells, vascular tissue and sheets of pigment epithelial cells lacking the distribution and organization of the normal retina and retinal pigment epithelium. The lesion is most commonly found unilaterally as a slightly elevated mass in a peripapillary location but can also occur in the macula or the retinal periphery. It is sometimes associated with neurofibromatosis type 1 or 2, nevoid basal cell carcinoma syndrome, or branchio-oculo-facial syndrome. Patients may be asymptomatic or present with progressive loss of vision. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5066128015 | A rare benign eye tumour characterised by the presence of glial cells, vascular tissue and sheets of pigment epithelial cells lacking the distribution and organisation of the normal retina and retinal pigment epithelium. The lesion is most commonly found unilaterally as a slightly elevated mass in a peripapillary location but can also occur in the macula or the retinal periphery. It is sometimes associated with neurofibromatosis type 1 or 2, naevoid basal cell carcinoma syndrome, or branchio-oculo-facial syndrome. Patients may be asymptomatic or present with progressive loss of vision. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Combined hamartoma of retina and retinal pigment epithelium | Is a | Subretinal lesion | true | Inferred relationship | Some | ||
| Combined hamartoma of retina and retinal pigment epithelium | Is a | Hamartoma of retina (disorder) | true | Inferred relationship | Some | ||
| Combined hamartoma of retina and retinal pigment epithelium | Is a | Retinal pigment epithelial abnormality | false | Inferred relationship | Some | ||
| Combined hamartoma of retina and retinal pigment epithelium | Finding site | Structure of retinal pigment epithelium | true | Inferred relationship | Some | 1 | |
| Combined hamartoma of retina and retinal pigment epithelium | Associated morphology | Hamartoma | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR