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 |
| 3657755015 | Male infertility with oligozoospermia due to single gene mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3657756019 | Male infertility with oligozoospermia due to single gene mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4651792018 | Male infertility with oligospermia due to single gene mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3657757011 | A rare genetic male infertility due to oligozoospermia (number of sperm in the ejaculate inferior to 15 million/mL) resulting from a mutation in a single gene known to cause oligozoospermia. Sperm morphology may be normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Male infertility with oligozoospermia due to single gene mutation | est un(e) (attribut) | Disorder of male genital organ (disorder) | true | Inferred relationship | Some | ||
| Male infertility with oligozoospermia due to single gene mutation | Due to | Genetic mutation (finding) | true | Inferred relationship | Some | 3 | |
| Male infertility with oligozoospermia due to single gene mutation | est un(e) (attribut) | Male infertility of genetic origin | true | Inferred relationship | Some | ||
| Male infertility with oligozoospermia due to single gene mutation | interprète (attribut) | Fertility, function (observable entity) | true | Inferred relationship | Some | 5 | |
| Male infertility with oligozoospermia due to single gene mutation | Due to | anomalie chromosomique | false | Inferred relationship | Some | 3 | |
| Male infertility with oligozoospermia due to single gene mutation | est un(e) (attribut) | Male reproductive finding | false | Inferred relationship | Some | ||
| Male infertility with oligozoospermia due to single gene mutation | interprète (attribut) | Male reproductive function | true | Inferred relationship | Some | 4 | |
| Male infertility with oligozoospermia due to single gene mutation | est un(e) (attribut) | Male infertility of chromosomal origin | false | Inferred relationship | Some | ||
| Male infertility with oligozoospermia due to single gene mutation | est un(e) (attribut) | Male genital organ disorder associated with another disorder (disorder) | false | Inferred relationship | Some | ||
| Male infertility with oligozoospermia due to single gene mutation | est un(e) (attribut) | Oligozoospermia | true | Inferred relationship | Some | ||
| Male infertility with oligozoospermia due to single gene mutation | interprète (attribut) | Concentration of sperm | true | Inferred relationship | Some | 1 | |
| Male infertility with oligozoospermia due to single gene mutation | localisation d'une constatation (attribut) | organes génitaux masculins | true | Inferred relationship | Some | 2 | |
| Male infertility with oligozoospermia due to single gene mutation | a pour interprétation (attribut) | Decreased | true | Inferred relationship | Some | 1 | |
| Male infertility with oligozoospermia due to single gene mutation | survenue (attribut) | congénital | false | Inferred relationship | Some | 4 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
Description inactivation indicator reference set
FHIR