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 |
| 768181000241111 | isochromosomie Yp (trouble) | fr | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 959741000172116 | isochromosomie Yp | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation 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 | est un(e) (attribut) | Anomaly of chromosome Y | true | Inferred relationship | Some | ||
| Isochromosomy Yp | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Isochromosomy Yp | morphologie associée (attribut) | Abnormal cell structure | true | Inferred relationship | Some | 1 | |
| Isochromosomy Yp | localisation d'une constatation (attribut) | Sex chromosome Y | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR