Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3736319012 | Congenital pontocerebellar hypoplasia type 9 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3736320018 | Congenital pontocerebellar hypoplasia type 9 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4611841015 | A rare genetic subtype of non-syndromic pontocerebellar hypoplasia with characteristics of progressive cerebellum and brainstem atrophy, corpus callosum hypo/aplasia and progressive post-natal microcephaly. Patients typically present profound global developmental delay, spastic tetraparesis, seizures, cortical visual impairment and on neuroimaging abnormal brain morphology that includes pontocerebellar hypoplasia, figure of 8 midbrain appearance and more variably interhemispheric cysts, ventriculomegaly and cerebral dysmyelination. There is evidence the disease is caused by homozygous mutation in the AMPD2 gene on chromosome 1p13. | 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 9 (disorder) | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 9 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 9 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 9 (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 9 (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 9 (disorder) | Finding site | Pontine structure | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 9 (disorder) | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 9 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 9 (disorder) | Finding site | Cerebellar structure | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 9 (disorder) | Is a | Congenital pontocerebellar hypoplasia | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 9 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 9 (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets