Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3644052014 | Morvan syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3644053016 | Morvan syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3644055011 | Limbic encephalitis, neuromyotonia, hyperhidrosis, polyneuropathy syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3644056012 | Morvan fibrillary chorea | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5404218014 | Morvan syndrome is a rare, life-threatening, acquired neurologic disease characterized by neuromyotonia, dysautonomia and encephalopathy with severe insomnia. Signs involving central (e.g. hallucinations, confusion, amnesia, myoclonus), autonomic (e.g. variations in blood pressure, hyperhidrosis) and peripheral (e.g. painful cramps, myokymia) hyperactivity, as well as systemic manifestations (such as weight loss, pruritus, fever), are reported. Thymoma is present in some cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5404219018 | Morvan syndrome is a rare, life-threatening, acquired neurologic disease characterised by neuromyotonia, dysautonomia and encephalopathy with severe insomnia. Signs involving central (e.g. hallucinations, confusion, amnesia, myoclonus), autonomic (e.g. variations in blood pressure, hyperhidrosis) and peripheral (e.g. painful cramps, myokymia) hyperactivity, as well as systemic manifestations (such as weight loss, pruritus, fever), are reported. Thymoma is present in some cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3644052014 | Morvan syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3644053016 | Morvan syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3644055011 | Limbic encephalitis, neuromyotonia, hyperhidrosis, polyneuropathy syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3644056012 | Morvan fibrillary chorea | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3644054010 | A rare life threatening acquired neurologic disease with characteristics of neuromyotonia, dysautonomia and encephalopathy with severe insomnia. Signs involving central (e.g. hallucinations, confusion, amnesia, myoclonus), autonomic (e.g. variations in blood pressure, hyperhidrosis) and peripheral (e.g. painful cramps, myokymia) hyperactivity, as well as systemic manifestations (such as weight loss, pruritus, fever), are reported. Thymoma is present in some cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5404218014 | Morvan syndrome is a rare, life-threatening, acquired neurologic disease characterized by neuromyotonia, dysautonomia and encephalopathy with severe insomnia. Signs involving central (e.g. hallucinations, confusion, amnesia, myoclonus), autonomic (e.g. variations in blood pressure, hyperhidrosis) and peripheral (e.g. painful cramps, myokymia) hyperactivity, as well as systemic manifestations (such as weight loss, pruritus, fever), are reported. Thymoma is present in some cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5404219018 | Morvan syndrome is a rare, life-threatening, acquired neurologic disease characterised by neuromyotonia, dysautonomia and encephalopathy with severe insomnia. Signs involving central (e.g. hallucinations, confusion, amnesia, myoclonus), autonomic (e.g. variations in blood pressure, hyperhidrosis) and peripheral (e.g. painful cramps, myokymia) hyperactivity, as well as systemic manifestations (such as weight loss, pruritus, fever), are reported. Thymoma is present in some cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3425051001000114 | Morvan-Syndrom | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
959441000172110 | chorée fibrillaire de Morvan | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
999841000172116 | syndrome de Morvan | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
959441000172110 | chorée fibrillaire de Morvan | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
999841000172116 | syndrome de Morvan | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3425051001000114 | Morvan-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 |
Morvan syndrome (disorder) | Is a | Movement disorder | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Morvan syndrome (disorder) | Is a | Disorder of brain | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Morvan syndrome (disorder) | Is a | Peripheral nerve disease | true | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
Morvan syndrome (disorder) | Finding site | Brain structure | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
Morvan syndrome (disorder) | Finding site | Peripheral nerve structure | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 2 | |
Morvan syndrome (disorder) | Interprets | Movement | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)