Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3424234017 | Familial multiple fibrofolliculoma (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3424235016 | Familial multiple fibrofolliculoma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3424236015 | A genodermatosis with characteristics of the presence of multiple hamartomas of the hair follicle. It has been described in one family so far. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial multiple fibrofolliculoma (disorder) | Is a | Autosomal dominant hereditary disorder | false | Inferred relationship | Some | ||
| Familial multiple fibrofolliculoma (disorder) | Is a | Familial neoplastic disease | false | Inferred relationship | Some | ||
| Familial multiple fibrofolliculoma (disorder) | Is a | Genodermatosis | false | Inferred relationship | Some | ||
| Familial multiple fibrofolliculoma (disorder) | Is a | Fibrofolliculoma | false | Inferred relationship | Some | ||
| Familial multiple fibrofolliculoma (disorder) | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
| Familial multiple fibrofolliculoma (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| Familial multiple fibrofolliculoma (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
| Familial multiple fibrofolliculoma (disorder) | Associated morphology | Follicular fibroma | false | Inferred relationship | Some | 2 | |
| Familial multiple fibrofolliculoma (disorder) | Finding site | Hair follicle structure | false | Inferred relationship | Some | 2 | |
| Familial multiple fibrofolliculoma (disorder) | Associated morphology | Developmental anomaly (morphologic abnormality) | false | Inferred relationship | Some | 3 | |
| Familial multiple fibrofolliculoma (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 3 | |
| Familial multiple fibrofolliculoma (disorder) | Associated morphology | Follicular fibroma | false | Inferred relationship | Some | 1 | |
| Familial multiple fibrofolliculoma (disorder) | Finding site | Hair follicle structure | false | Inferred relationship | Some | 1 | |
| Familial multiple fibrofolliculoma (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Familial multiple fibrofolliculoma (disorder) | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
REPLACED BY association reference set (foundation metadata concept)
FHIR