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 |
| 3646027014 | Male infertility with teratozoospermia due to single gene mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3646028016 | Male infertility with teratozoospermia due to single gene mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 766781000241114 | infertilité masculine monogénique avec tératozoospermie (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 939981000172110 | infertilité masculine monogénique avec tératozoospermie | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3646030019 | A rare genetic male infertility due to sperm disorder with characteristics of the presence of spermatozoa with abnormal morphology, such as macrozoospermia or globozoospermia, in over 85% of sperm, resulting from mutation in a single gene known to cause teratozoospermia. It is a heterogeneous group that includes a wide range of abnormal sperm phenotypes affecting, solely or simultaneously, head, neck, midpiece and/or tail. | 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 teratozoospermia due to single gene mutation (disorder) | est un(e) (attribut) | Male infertility of genetic origin | true | Inferred relationship | Some | ||
| Male infertility with teratozoospermia due to single gene mutation (disorder) | est un(e) (attribut) | Disorder of male genital organ (disorder) | true | Inferred relationship | Some | ||
| Male infertility with teratozoospermia due to single gene mutation (disorder) | interprète (attribut) | Fertility, function (observable entity) | true | Inferred relationship | Some | 2 | |
| Male infertility with teratozoospermia due to single gene mutation (disorder) | Due to | anomalie chromosomique | false | Inferred relationship | Some | 4 | |
| Male infertility with teratozoospermia due to single gene mutation (disorder) | est un(e) (attribut) | Male infertility of chromosomal origin | false | Inferred relationship | Some | ||
| Male infertility with teratozoospermia due to single gene mutation (disorder) | est un(e) (attribut) | Teratozoospermia (disorder) | true | Inferred relationship | Some | ||
| Male infertility with teratozoospermia due to single gene mutation (disorder) | interprète (attribut) | Male reproductive function | true | Inferred relationship | Some | 3 | |
| Male infertility with teratozoospermia due to single gene mutation (disorder) | interprète (attribut) | Evaluation of spermatozoa morphology | true | Inferred relationship | Some | 5 | |
| Male infertility with teratozoospermia due to single gene mutation (disorder) | interprète (attribut) | entité observable du sperme | true | Inferred relationship | Some | 4 | |
| Male infertility with teratozoospermia due to single gene mutation (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 5 | |
| Male infertility with teratozoospermia due to single gene mutation (disorder) | est un(e) (attribut) | Male genital organ disorder associated with another disorder (disorder) | false | Inferred relationship | Some | ||
| Male infertility with teratozoospermia due to single gene mutation (disorder) | localisation d'une constatation (attribut) | organes génitaux masculins | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR