Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3763701017 | Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3763702012 | Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3763703019 | Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3763704013 | A rare genetic non-syndromic cerebral malformation due to abnormal neuronal migration disease with the association of cortical dysplasia and pontocerebellar hypoplasia, manifesting with global developmental delay, mild to severe intellectual disability, axial hypotonia, strabismus, nystagmus and occasionally, optic nerve hypoplasia. Brain imaging reveals variable malformations, including frontally predominant microgyria, gyral disorganization and simplification, dysmorphic and hypertrophic basal ganglia, cerebellar vermis dysplasia, brainstem/corpus callosum hypoplasia, and/or olfactory bulbs agenesis. Caused by heterozygous mutation in the TUBB3 gene on chromosome 16q24. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3763705014 | A rare genetic non-syndromic cerebral malformation due to abnormal neuronal migration disease with the association of cortical dysplasia and pontocerebellar hypoplasia, manifesting with global developmental delay, mild to severe intellectual disability, axial hypotonia, strabismus, nystagmus and occasionally, optic nerve hypoplasia. Brain imaging reveals variable malformations, including frontally predominant microgyria, gyral disorganisation and simplification, dysmorphic and hypertrophic basal ganglia, cerebellar vermis dysplasia, brainstem/corpus callosum hypoplasia, and/or olfactory bulbs agenesis. Caused by heterozygous mutation in the TUBB3 gene on chromosome 16q24. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4339791000052116 | kortikal dysgenesi med pontocerebellär hypoplasi orsakad av TUBB3-mutation | sv | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 2 | |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Finding site | Cerebellar structure | true | Inferred relationship | Some | 2 | |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Is a | Cortical dysplasia | true | Inferred relationship | Some | ||
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Is a | Congenital pontocerebellar hypoplasia | true | Inferred relationship | Some | ||
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 3 | |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Finding site | Structure of cerebral cortex (body structure) | true | Inferred relationship | Some | 1 | |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Finding site | Pontine structure | true | Inferred relationship | Some | 3 | |
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets