Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3758314017 | Familial dementia Danish type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3758315016 | ADan amyloidosis | en | Synonym | Active | Case sensitive | SNOMED CT core |
3758316015 | Familial dementia Danish type (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3758317012 | A rare neurodegenerative disease with characteristics of progressive cataracts, hearing loss, cerebellar ataxia, paranoid psychosis and dementia. Neuropathological features are diffuse atrophy of all parts of the brain, chronic diffuse encephalopathy and the presence of extremely thin and almost completely demyelinated cranial nerves. Caused by mutation in the ITM2B gene. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Mental health disorder reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set