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 |
| 3662335013 | Isochromosomy Yp | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3662336014 | Isochromosome Yp | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3662337017 | Isochromosomy Yp (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 8477161000146114 | isochromosomie Yp | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 8477171000146115 | isochromosomie Yp (aandoening) | nl | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3662338010 | Isochromosomy Yp is a rare gonosome anomaly characterised by various clinical presentations including normal healthy fertile males, male phenotype with infertility, and males with ambiguous genitalia or incomplete masculinisation. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3662339019 | Isochromosomy Yp is a rare gonosome anomaly characterized by various clinical presentations including normal healthy fertile males, male phenotype with infertility, and males with ambiguous genitalia or incomplete masculinization. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Isochromosomy Yp | Is a | Anomaly of chromosome Y | true | Inferred relationship | Some | ||
| Isochromosomy Yp | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Isochromosomy Yp | Associated morphology | Abnormal cell structure | true | Inferred relationship | Some | 1 | |
| Isochromosomy Yp | Finding site | Sex chromosome Y | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
FHIR