Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4168246015 | Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation | en | Synonym | Active | Case sensitive | SNOMED CT core |
4168247012 | Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation | en | Synonym | Active | Case sensitive | SNOMED CT core |
4168248019 | Leydig cell hypoplasia due to partial LH receptor inactivation | en | Synonym | Active | Case sensitive | SNOMED CT core |
4168249010 | Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
4164767014 | This is a rare autosomal recessive genetic and endocrine syndrome, characterised by a partial 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 | Case sensitive | SNOMED CT core |
4283399015 | This is a rare autosomal recessive genetic and endocrine syndrome, characterized by a partial 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 | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation | Is a | Leydig cell agenesis | true | Inferred relationship | Some | ||
Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation | Finding site | Structure of interstitial cell of Leydig | true | Inferred relationship | Some | 1 | |
Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set