Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3498781017 | Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3498782012 | Chang Davidson Carlson syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3498783019 | Hypogonadotropic hypogonadism retinitis pigmentosa syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3957491000052110 | syndrom med hypogonadotrop hypogonadism och retinitis pigmentosa | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
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 (disorder) | 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 (disorder) | 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 pars distalis of pituitary (body structure) | true | Inferred relationship | Some | 5 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets