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 |
5402956015 | This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402957012 | This syndrome is characterised by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3332220011 | Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3332226017 | Male hypergonadotropic hypogonadism, intellectual disability, skeletal anomaly syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3332227014 | Sohval Soffer syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
883521000172117 | syndrome d'hypogonadisme hypergonadotrope masculin-déficience intellectuelle-anomalies squelettiques | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
934841000172113 | syndrome de Sohval-Soffer | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3429651001000115 | Männlicher Hypogonadismus-Intelligenzminderung-Skelettanomalien-Syndrom | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Is a | Congenital anomaly of skeletal bone | true | Inferred relationship | Some | ||
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Is a | Multiple system malformation syndrome | true | Inferred relationship | Some | ||
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Is a | retard mental | false | Inferred relationship | Some | ||
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Is a | X-linked hereditary disease | true | Inferred relationship | Some | ||
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Is a | Connective tissue hereditary disorder | false | Inferred relationship | Some | ||
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Is a | Reproductive system hereditary disorder | true | Inferred relationship | Some | ||
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Is a | Primary testicular failure (disorder) | true | Inferred relationship | Some | ||
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Finding site | Testicular endocrine structure | false | Inferred relationship | Some | ||
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Has definitional manifestation | Decreased hormone production | false | Inferred relationship | Some | ||
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Associated morphology | anomalie du développement | false | Inferred relationship | Some | 3 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Finding site | Bone structure | true | Inferred relationship | Some | 3 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Finding site | Testicular endocrine structure | true | Inferred relationship | Some | 1 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Has interpretation | Decreased | true | Inferred relationship | Some | 2 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Interprets | Hormone production | true | Inferred relationship | Some | 2 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Is a | Intellectual disability | false | Inferred relationship | Some | ||
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 3 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Interprets | Intellectual ability | true | Inferred relationship | Some | 4 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Has interpretation | Impaired | true | Inferred relationship | Some | 4 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 5 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Has interpretation | Impaired | true | Inferred relationship | Some | 5 | |
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus. | Is a | Genetic intellectual disability | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)