Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2989585014 | Ulnar mammary syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2989606017 | Ulnar mammary syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2989640017 | Ulnar-mammary syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2989657018 | Schinzel syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 2989692014 | An extremely rare inherited disorder characterized by malformations of the ulnar ray, hypoplasia and dysfunction of the axillary apocrine and mammary glands, endocrine dysfunction, dental anomalies, and occasional visceral malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3776280014 | An extremely rare inherited disorder characterised by malformations of the ulnar ray, hypoplasia and dysfunction of the axillary apocrine and mammary glands, endocrine dysfunction, dental anomalies, and occasional visceral malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Ulnar mammary syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Ulnar mammary syndrome | Is a | Anomaly of chromosome pair 12 | true | Inferred relationship | Some | ||
| Ulnar mammary syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Ulnar mammary syndrome | Associated morphology | Cellular AND/OR subcellular abnormality | true | Inferred relationship | Some | 1 | |
| Ulnar mammary syndrome | Finding site | Chromosome pair 12 | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR