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 |
| 3727850017 | Familial angiolipomatosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3727851018 | Familial angiolipomatosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 6220481000146118 | familiaire angiolipomatose | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6220501000146114 | familiaire angiolipomatose (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6866211000146110 | familiale angiolipomatose | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3727852013 | A rare genetic subcutaneous tissue disorder with the presence of benign usually multiple subcutaneous tumors. The tumors are composed of adipose tissue and blood vessels typically manifesting as yellow firm circumscribed 1-4 cm in diameter tumors located in the arms, legs and trunk with deep extension of the lesions between muscles, tendons and joint capsules (without infiltration of these structures) in several members of a single family. Tumors may be tender or mildly painful when palpated and do not regress spontaneously. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3727853015 | A rare genetic subcutaneous tissue disorder with the presence of benign usually multiple subcutaneous tumours. The tumours are composed of adipose tissue and blood vessels typically manifesting as yellow firm circumscribed 1-4 cm in diameter tumours located in the arms, legs and trunk with deep extension of the lesions between muscles, tendons and joint capsules (without infiltration of these structures) in several members of a single family. Tumours may be tender or mildly painful when palpated and do not regress spontaneously. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial angiolipomatosis | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
| Familial angiolipomatosis | Finding site | Subcutaneous tissue structure | true | Inferred relationship | Some | 1 | |
| Familial angiolipomatosis | Is a | Angiolipoma (disorder) | true | Inferred relationship | Some | ||
| Familial angiolipomatosis | Associated morphology | Angiolipoma | true | Inferred relationship | Some | 1 | |
| Familial angiolipomatosis | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Familial angiolipomatosis | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
| Familial angiolipomatosis | Is a | Familial neoplastic disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR