Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3705539018 | Hereditary progressive mucinous histiocytosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3705540016 | Hereditary progressive mucinous histiocytosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3705541017 | A rare benign non-Langerhans cell histiocytosis characterized by childhood or adolescence onset of multiple, small, asymptomatic, slowly progressing, skin-colored to red-brown papules with predilection for the face, dorsal hands, forearms and legs, without associated mucosal or visceral involvement. Histologically, papules are well-circumscribed, unencapsulated, nodular aggregates of histiocytes with abundant mucin in the upper and mid dermis. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3705542012 | A rare benign non-Langerhans cell histiocytosis characterised by childhood or adolescence onset of multiple, small, asymptomatic, slowly progressing, skin-coloured to red-brown papules with predilection for the face, dorsal hands, forearms and legs, without associated mucosal or visceral involvement. Histologically, papules are well-circumscribed, unencapsulated, nodular aggregates of histiocytes with abundant mucin in the upper and mid dermis. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary progressive mucinous histiocytosis | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 | |
| Hereditary progressive mucinous histiocytosis | Is a | Chronic disease of skin | true | Inferred relationship | Some | ||
| Hereditary progressive mucinous histiocytosis | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
| Hereditary progressive mucinous histiocytosis | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
| Hereditary progressive mucinous histiocytosis | Associated morphology | Mucinous histiocytosis | true | Inferred relationship | Some | 1 | |
| Hereditary progressive mucinous histiocytosis | Is a | Non-Langerhans cell histiocytic dermatosis (disorder) | true | Inferred relationship | Some | ||
| Hereditary progressive mucinous histiocytosis | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Hereditary progressive mucinous histiocytosis | Is a | Chronic histiocytosis | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR