Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3312932010 | Congenital pontocerebellar hypoplasia type 8 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3312933017 | Congenital pontocerebellar hypoplasia type 8 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3312934011 | PCH8 - pontocerebellar hypoplasia type 8 | en | Synonym | Active | Case sensitive | SNOMED CT core |
3312935012 | Pontocerebellar hypoplasia type 8 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3312936013 | Pontocerebellar hypoplasia due to CHMP1A (charged multivesicular body protein 1A) mutation | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3312906016 | A novel very rare form of PCH with clinical manifestations of progressive microcephaly, feeding difficulties and severe developmental delay. Although walking may be achieved, hypotonia often associated with increased muscle tone of lower extremities and deep tendon reflexes, joint deformities in the lower extremities, and occasionally complex seizures are demonstrated. PCH8 is caused by a loss-of-function mutation in the CHMP1A gene. | 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