Status: current, Primitive. Date: 31-Mar 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4964768013 | Progressive cerebello-cerebral atrophy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4964769017 | Progressive cerebello-cerebral atrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
4964770016 | PCCA - progressive cerebello-cerebral atrophy | en | Synonym | Active | Case sensitive | SNOMED CT core |
5155241015 | A rare genetic neurological disorder with characteristics of postnatal onset of severe global developmental delay, profound intellectual disability, progressive microcephaly, progressive spasticity evolving into spastic quadriplegia with joint contractures, generalized seizures and irritability. Severe choreoathetosis and dysmorphic features are absent. Brain imaging shows progressive cerebellar atrophy followed by cerebral atrophy affecting both white and gray matter without pontine involvement. | en | Definition | Active | Case sensitive | SNOMED CT core |
5155242010 | A rare genetic neurological disorder with characteristics of postnatal onset of severe global developmental delay, profound intellectual disability, progressive microcephaly, progressive spasticity evolving into spastic quadriplegia with joint contractures, generalised seizures and irritability. Severe choreoathetosis and dysmorphic features are absent. Brain imaging shows progressive cerebellar atrophy followed by cerebral atrophy affecting both white and grey matter without pontine involvement. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set