Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 6067019 | Paget's disease, mammary | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 6068012 | Paget's disease of breast | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 6069016 | Paget's carcinoma of the nipple | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 760790016 | Paget's disease, mammary (morphologic abnormality) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
| 1226519014 | Mammary Paget's disease | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 2838268016 | Paget disease, mammary | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Paget's disease, mammary | Is a | Malignant neoplasm, primary | false | Inferred relationship | Existential restriction modifier | ||
| Paget's disease, mammary | Is a | Ductal, lobular AND/OR medullary neoplasm | false | Inferred relationship | Existential restriction modifier | ||
| Paget's disease, mammary | Pathological process | Malignant neoplastic process | false | Inferred relationship | Existential restriction modifier | ||
| Paget's disease, mammary | Is a | Paget's disease of skin | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Paget's disease of nipple | Associated morphology | False | Paget's disease, mammary | Inferred relationship | Existential restriction modifier | 1 |
| Paget's disease of nipple | Associated morphology | True | Paget's disease, mammary | Inferred relationship | Existential restriction modifier | 1 |
This concept is not in any reference sets
FHIR