Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3433638013 | Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3433639017 | Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3433640015 | Hypomyelinating leucodystrophy with atrophy of basal ganglia and cerebellum | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3433641016 | H-ABC - hypomyelination, atrophy of basal ganglia and cerebellum | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3433642011 | Hypomyelination with atrophy of basal ganglia and cerebellum syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5403304014 | A rare disorder characterized by slowly progressive spasticity, extrapyramidal movement disorders (dystonia, choreoathetosis and rigidity), cerebellar ataxia, moderate to severe cognitive deficit, and anarthria/dysarthria. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403305010 | A rare disorder characterised by slowly progressive spasticity, extrapyramidal movement disorders (dystonia, choreoathetosis and rigidity), cerebellar ataxia, moderate to severe cognitive deficit, and anarthria/dysarthria. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Is a | Congenital anomaly of brain | false | Inferred relationship | Some | ||
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Is a | Disorder of basal ganglia (disorder) | true | Inferred relationship | Some | ||
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Is a | Leucodystrophy | false | Inferred relationship | Some | ||
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Is a | Cerebellar disorder | false | Inferred relationship | Some | ||
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Is a | Cerebral atrophy | true | Inferred relationship | Some | ||
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 4 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Associated morphology | Atrophy | false | Inferred relationship | Some | 5 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 5 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Finding site | Cerebellar structure | false | Inferred relationship | Some | 5 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 7 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Associated morphology | Atrophy | false | Inferred relationship | Some | 7 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Finding site | Basal ganglion structure (body structure) | false | Inferred relationship | Some | 7 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Associated morphology | Hypomyelination | false | Inferred relationship | Some | 4 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 4 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Finding site | Brain structure | false | Inferred relationship | Some | 4 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 6 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Associated morphology | Myelin sheath alteration | false | Inferred relationship | Some | 6 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Finding site | Structure of nervous system (body structure) | false | Inferred relationship | Some | 6 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Is a | Cerebellar ataxia | true | Inferred relationship | Some | ||
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Is a | Hereditary ataxia (disorder) | true | Inferred relationship | Some | ||
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Finding site | White matter structure of brain and spinal cord (body structure) | true | Inferred relationship | Some | 4 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Is a | TUBB4A-related leukodystrophy | true | Inferred relationship | Some | ||
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 3 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Finding site | Cerebellar structure | true | Inferred relationship | Some | 3 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Finding site | Basal ganglion structure (body structure) | true | Inferred relationship | Some | 1 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Associated morphology | Atrophy | true | Inferred relationship | Some | 1 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Associated morphology | Myelin sheath alteration | true | Inferred relationship | Some | 2 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Finding site | Myelinated nerve fiber structure | true | Inferred relationship | Some | 2 | |
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) | Is a | Hereditary cerebellar degeneration | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)