Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3646045014 | Intraosseous hemangioma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3646046010 | Intraosseous haemangioma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3646047018 | Primary intraosseous venous malformation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3646048011 | Osseous venous malformation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3646049015 | Primary intraosseous venous malformation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3646051016 | A rare genetic vascular anomaly with characteristics of severe blood vessel expansion most frequently within the craniofacial bones with painless bone enlargement usually of mandibula, maxilla and/or orbital, nasal and frontal bones. This typically results in facial asymmetry and contour deformation. Midline abnormalities, such as diastasis recti, supraumbilical raphe, and hiatus hernia, are commonly associated. Additional features reported include gingival bleeding, ectopic tooth eruption, exophthalmos and loss of vision, nausea, and vomiting. There is evidence the disease is caused by homozygous mutation in the ELMO2 gene on chromosome 20q13. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Primary intraosseous venous malformation (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Primary intraosseous venous malformation (disorder) | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| Primary intraosseous venous malformation (disorder) | Is a | Infantile haemangioma of rare localisation | true | Inferred relationship | Some | ||
| Primary intraosseous venous malformation (disorder) | Is a | Congenital hemangioma | true | Inferred relationship | Some | ||
| Primary intraosseous venous malformation (disorder) | Associated morphology | Benign hemangioma | true | Inferred relationship | Some | 1 | |
| Primary intraosseous venous malformation (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Primary intraosseous venous malformation (disorder) | Finding site | Blood vessel structure (body structure) | true | Inferred relationship | Some | 1 | |
| Primary intraosseous venous malformation (disorder) | Is a | Mass of cardiovascular structure | false | Inferred relationship | Some | ||
| Primary intraosseous venous malformation (disorder) | Is a | Congenital vascular disorder (disorder) | false | Inferred relationship | Some | ||
| Primary intraosseous venous malformation (disorder) | Is a | Lesion of soft tissue (disorder) | false | Inferred relationship | Some | ||
| Primary intraosseous venous malformation (disorder) | Is a | Mass of soft tissue (finding) | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR