Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3313157011 | Deafness and hypogonadism syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3313305019 | Deafness and hypogonadism syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401825013 | A rare form of syndromic genetic deafness characterized by the association of congenital mixed hearing loss with perilymphatic gusher (Gusher syndrome or DFN3), hypogonadism and abnormal behavior. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401826014 | A rare form of syndromic genetic deafness characterised by the association of congenital mixed hearing loss with perilymphatic gusher (Gusher syndrome or DFN3), hypogonadism and abnormal behaviour. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Deafness and hypogonadism syndrome (disorder) | Is a | Hypogonadism | true | Inferred relationship | Some | ||
Deafness and hypogonadism syndrome (disorder) | Is a | X-linked hereditary disease | false | Inferred relationship | Some | ||
Deafness and hypogonadism syndrome (disorder) | Is a | Hearing loss associated with syndrome | true | Inferred relationship | Some | ||
Deafness and hypogonadism syndrome (disorder) | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
Deafness and hypogonadism syndrome (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
Deafness and hypogonadism syndrome (disorder) | Is a | Reproductive system hereditary disorder | true | Inferred relationship | Some | ||
Deafness and hypogonadism syndrome (disorder) | Finding site | Ear structure | false | Inferred relationship | Some | ||
Deafness and hypogonadism syndrome (disorder) | Finding site | Gonadal endocrine structure | false | Inferred relationship | Some | ||
Deafness and hypogonadism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Deafness and hypogonadism syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Deafness and hypogonadism syndrome (disorder) | Finding site | Gonadal endocrine structure | true | Inferred relationship | Some | 1 | |
Deafness and hypogonadism syndrome (disorder) | Finding site | Ear structure | true | Inferred relationship | Some | 2 | |
Deafness and hypogonadism syndrome (disorder) | Is a | Congenital hearing disorder | true | Inferred relationship | Some | ||
Deafness and hypogonadism syndrome (disorder) | Is a | Disorder of ear | true | Inferred relationship | Some | ||
Deafness and hypogonadism syndrome (disorder) | Interprets | Hearing | true | Inferred relationship | Some | 3 | |
Deafness and hypogonadism syndrome (disorder) | Is a | X-linked recessive hereditary disease | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)