Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3498781017 | Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3498782012 | Chang Davidson Carlson syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3498783019 | Hypogonadotropic hypogonadism retinitis pigmentosa syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3499981015 | This syndrome is characterized by the association of hypogonadotropic hypogonadism (with primary amenorrhea and lack of secondary sexual development) and retinitis pigmentosa. It has been described in two sisters born to nonconsanguineous parents. | en | Definition | Active | Case sensitive | SNOMED CT core |
3499982010 | This syndrome is characterised by the association of hypogonadotropic hypogonadism (with primary amenorrhoea and lack of secondary sexual development) and retinitis pigmentosa. It has been described in two sisters born to nonconsanguineous parents. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | Is a | Retinitis pigmentosa | true | Inferred relationship | Some | ||
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Some | ||
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | Is a | Reproductive system hereditary disorder | true | Inferred relationship | Some | ||
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | Is a | Congenital hypogonadotropic hypogonadism | true | Inferred relationship | Some | ||
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | Associated morphology | Dystrophy | true | Inferred relationship | Some | 3 | |
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | Finding site | Retinal structure | true | Inferred relationship | Some | 3 | |
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 4 | |
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 5 | |
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | Finding site | Gonadal endocrine structure | true | Inferred relationship | Some | 4 | |
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | Finding site | Structure of distal part of pituitary | true | Inferred relationship | Some | 5 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set