Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3312933017 | Congenital pontocerebellar hypoplasia type 8 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3312934011 | PCH8 - pontocerebellar hypoplasia type 8 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3312935012 | Pontocerebellar hypoplasia type 8 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3312936013 | Pontocerebellar hypoplasia due to CHMP1A (charged multivesicular body protein 1A) mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5401794013 | Pontocerebellar hypoplasia type 8 (PCH8) is a novel very rare form of pontocerebellar hypoplasia characterized clinically by progressive microencephaly, feeding difficulties, 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. PCH8 is caused by a loss-of-function mutation in the CHMP1A gene. MRI demonstrates a pontocerebellar hypoplasia with vermis and hemispheres equally affected and mild to severely reduced cerebral white matter volume with a fully formed very thin corpus callosum. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401795014 | Pontocerebellar hypoplasia type 8 (PCH8) is a novel very rare form of pontocerebellar hypoplasia characterised clinically by progressive microencephaly, feeding difficulties, 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. PCH8 is caused by a loss-of-function mutation in the CHMP1A gene. MRI demonstrates a pontocerebellar hypoplasia with vermis and hemispheres equally affected and mild to severely reduced cerebral white matter volume with a fully formed very thin corpus callosum. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital pontocerebellar hypoplasia type 8 (disorder) | Is a | Congenital pontocerebellar hypoplasia | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 8 (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 8 (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 8 (disorder) | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 8 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 8 (disorder) | Finding site | Cerebellar structure | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 8 (disorder) | Associated morphology | Hypoplasia | false | Inferred relationship | Some | 3 | |
Congenital pontocerebellar hypoplasia type 8 (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Congenital pontocerebellar hypoplasia type 8 (disorder) | Finding site | Pontine structure | false | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 8 (disorder) | Finding site | Cerebellar structure | false | Inferred relationship | Some | 3 | |
Congenital pontocerebellar hypoplasia type 8 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 8 (disorder) | Finding site | Pontine structure | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 8 (disorder) | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 8 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 8 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 8 (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)