Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4593930016 | Congenital iodine deficiency syndrome of neurological type (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4593931017 | Congenital iodine deficiency syndrome of neurological type | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4594735012 | Endemic cretinism of neurological type | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
838191000052117 | medfött jodbristsyndrom, neurologisk typ | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital iodine deficiency syndrome of neurological type (disorder) | Is a | Endemic cretinism | true | Inferred relationship | Some | ||
Congenital iodine deficiency syndrome of neurological type (disorder) | Causative agent | Environmental agent | false | Inferred relationship | Some | ||
Congenital iodine deficiency syndrome of neurological type (disorder) | Associated morphology | medfödd brist | false | Inferred relationship | Some | ||
Congenital iodine deficiency syndrome of neurological type (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
Congenital iodine deficiency syndrome of neurological type (disorder) | Causative agent | Iodine | false | Inferred relationship | Some | ||
Congenital iodine deficiency syndrome of neurological type (disorder) | Finding site | Entire endocrine gonad (body structure) | false | Inferred relationship | Some | ||
Congenital iodine deficiency syndrome of neurological type (disorder) | Finding site | Thyroid structure | false | Inferred relationship | Some | 2 | |
Congenital iodine deficiency syndrome of neurological type (disorder) | Associated etiologic finding | Iodine deficiency | false | Inferred relationship | Some | ||
Congenital iodine deficiency syndrome of neurological type (disorder) | Associated morphology | medfödd missbildning | false | Inferred relationship | Some | ||
Congenital iodine deficiency syndrome of neurological type (disorder) | Due to | Iodine deficiency | false | Inferred relationship | Some | ||
Congenital iodine deficiency syndrome of neurological type (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital iodine deficiency syndrome of neurological type (disorder) | Associated morphology | utvecklingsabnormitet | false | Inferred relationship | Some | 1 | |
Congenital iodine deficiency syndrome of neurological type (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Congenital iodine deficiency syndrome of neurological type (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital iodine deficiency syndrome of neurological type (disorder) | Finding site | Thyroid structure | true | Inferred relationship | Some | 1 | |
Congenital iodine deficiency syndrome of neurological type (disorder) | Is a | Neurological finding | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital iodine deficiency syndrome of mixed type (disorder) | Is a | True | Congenital iodine deficiency syndrome of neurological type (disorder) | Inferred relationship | Some |
This concept is not in any reference sets