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 |
| 5048592016 | Familial multiple trichodiscoma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5048593014 | Familial multiple discoid fibroma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5048594015 | Familial multiple discoid fibroma (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 13553361000146113 | familiaire multipele folliculaire fibromen | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 13553371000146119 | familiaire multipele folliculaire fibromen (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 13553381000146117 | familiaire multipele perifolliculaire fibromen | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 13553391000146115 | familiaire multipele trichodiscomen | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 13553401000146117 | familiaire multipele fibrofolliculomen | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 5048595019 | A rare genetic skin tumour disorder characterised by childhood-onset of multiple benign asymptomatic white to flesh-coloured papules predominantly located on the face, ears, neck and trunk, not associated with systemic organ involvement, associated malignancies or FLCN gene locus mutation. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5048596018 | A rare genetic skin tumor disorder characterized by childhood-onset of multiple benign asymptomatic white to flesh-colored papules predominantly located on the face, ears, neck and trunk, not associated with systemic organ involvement, associated malignancies or FLCN gene locus mutation. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial multiple discoid fibroma | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Familial multiple discoid fibroma | Is a | Trichodiscoma | true | Inferred relationship | Some | ||
| Familial multiple discoid fibroma | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
| Familial multiple discoid fibroma | Is a | Dermatosis in childhood (disorder) | true | Inferred relationship | Some | ||
| Familial multiple discoid fibroma | Is a | Familial neoplastic disease | true | Inferred relationship | Some | ||
| Familial multiple discoid fibroma | Occurrence | Childhood | true | Inferred relationship | Some | 1 | |
| Familial multiple discoid fibroma | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
| Familial multiple discoid fibroma | Associated morphology | Follicular fibroma | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR