Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2995003017 | Familial isolated vitamin E deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2995019012 | Friedreich-like ataxia | en | Synonym | Active | Case sensitive | SNOMED CT core |
2995296010 | Ataxia with vitamin E deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
2995541017 | Ataxia with vitamin E deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2995595010 | Ataxia with isolated vitamin E deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2995915015 | Friedreich ataxia phenotype with selective vitamin E deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Ataxia with vitamin E deficiency | Is a | Nutritional ataxic neuropathy | true | Inferred relationship | Some | ||
Ataxia with vitamin E deficiency | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Ataxia with vitamin E deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Ataxia with vitamin E deficiency | Finding site | Nerve structure | false | Inferred relationship | Some | ||
Ataxia with vitamin E deficiency | Finding site | Peripheral nervous system structure | false | Inferred relationship | Some | ||
Ataxia with vitamin E deficiency | Due to | Vitamin deficiency | true | Inferred relationship | Some | 1 | |
Ataxia with vitamin E deficiency | Finding site | Peripheral nerve structure | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set