Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3312901014 | Congenital pontocerebellar hypoplasia type 6 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3312902019 | Congenital pontocerebellar hypoplasia type 6 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3312903012 | Pontocerebellar hypoplasia type 6 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3312904018 | PCH6 - pontocerebellar hypoplasia type 6 | en | Synonym | Active | Case sensitive | SNOMED CT core |
3312905017 | Fatal infantile encephalopathy with mitochondrial respiratory chain defect | en | Synonym | Active | Case insensitive | SNOMED CT core |
3312913016 | A rare form of pontocerebellar hypoplasia with characteristics at birth of hypotonia, clonus, epilepsy, impaired swallowing and from infancy progressive microcephaly, spasticity and lactic acidosis. Reported in less than 10 cases to date. Caused by missense and splice site mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene located to 6q16.1. Prognosis is poor, exact life expectancy is unknown but in most cases does not exceed infancy. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set