Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4168242018 | Leydig cell hypoplasia due to complete LH receptor inactivation | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4168243011 | Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4168244017 | Leydig cell hypoplasia due to complete luteinising hormone receptor inactivation | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4168245016 | Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4164764019 | This is a rare autosomal recessive genetic and endocrine syndrome, characterised by a complete inability of the body to respond to luteinising hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testosterone. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4283400010 | This is a rare autosomal recessive genetic and endocrine syndrome, characterized by a complete inability of the body to respond to luteinizing hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testosterone. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) | est un(e) (attribut) | Leydig cell agenesis (disorder) | true | Inferred relationship | Some | ||
| Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) | localisation d'une constatation (attribut) | Structure of interstitial cell of Leydig (cell structure) | true | Inferred relationship | Some | 1 | |
| Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) | morphologie associée (attribut) | Hypoplasia (morphologic abnormality) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR