Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Oct 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4643807011 | Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4643808018 | Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4643809014 | Congenital cerebellar ataxia due to RNU12 mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
4643810016 | A rare hereditary ataxia with characteristics of delayed motor milestones in early infancy, hypotonia, ataxic gait, intention tremor, nystagmus, dysarthric speech and variable learning difficulties. Neuroimaging shows a mixed picture of cerebellar hypoplasia and degeneration, with an almost absent inferior lobule and thinning of the folia of the vermis. In addition, cisterna magna and fourth ventricle are enlarged with relative sparing of the brain stem volume. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Is a | Hereditary ataxia (disorder) | true | Inferred relationship | Some | ||
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Is a | Cerebellar ataxia | true | Inferred relationship | Some | ||
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Is a | Congenital cerebellar hypoplasia | true | Inferred relationship | Some | ||
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 2 | |
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 2 | |
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 3 | |
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets