Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4008377013 | Klinefelter syndrome, male with 46,XX karyotype (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4008378015 | Klinefelter's syndrome, male with 46,XX karyotype | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4008379011 | Klinefelter syndrome, male with 46,XX karyotype | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 2478651000052113 | Klinefelters syndrom, man med 46 XX-karyotyp | sv | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Is a | XX males | true | Inferred relationship | Some | ||
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Finding site | Male structure | false | Inferred relationship | Some | ||
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Finding site | Sex chromosome X | false | Inferred relationship | Some | 1 | |
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Associated morphology | Alteration of chromosome structure | false | Inferred relationship | Some | ||
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Associated morphology | kongenital anomali | false | Inferred relationship | Some | 1 | |
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Finding site | Sex chromosome X | false | Inferred relationship | Some | 1 | |
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Associated morphology | kongenital anomali | false | Inferred relationship | Some | ||
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Associated morphology | Cellular AND/OR subcellular abnormality | false | Inferred relationship | Some | 1 | |
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Finding site | Sex chromosome X | false | Inferred relationship | Some | 1 | |
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Associated morphology | Chromosomal morphology | true | Inferred relationship | Some | 2 | |
| Klinefelter syndrome, male with 46,XX karyotype (disorder) | Finding site | Sex chromosome X | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR