Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Feb 2024. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5298497011 | Congenital pontocerebellar hypoplasia type 11 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5298498018 | Pontocerebellar hypoplasia due to TBC1D23 mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5298499014 | PCH11 - pontocerebellar hypoplasia type 11 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5298500017 | Congenital pontocerebellar hypoplasia type 11 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5298503015 | A form of pontocerebellar hypoplasia characterized by microcephaly, severe global developmental delay and intellectual disability, dysmorphic facial features, cerebellar syndrome, and pontocerebellar hypoplasia on brain imaging. Behavioral abnormalities are frequently observed. Other reported manifestations include seizures, ocular anomalies, recurrent respiratory infections, and thin or absent corpus callosum, among others. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5298504014 | A form of pontocerebellar hypoplasia characterised by microcephaly, severe global developmental delay and intellectual disability, dysmorphic facial features, cerebellar syndrome, and pontocerebellar hypoplasia on brain imaging. Behavioural abnormalities are frequently observed. Other reported manifestations include seizures, ocular anomalies, recurrent respiratory infections, and thin or absent corpus callosum, among others. | 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 11 (disorder) | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 11 (disorder) | Is a | Microcephaly (finding) | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 11 (disorder) | Is a | Global developmental delay | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 11 (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 11 (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 11 (disorder) | Is a | Congenital pontocerebellar hypoplasia | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 11 (disorder) | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 11 (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Congenital pontocerebellar hypoplasia type 11 (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 4 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 4 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 5 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 5 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Interprets | Head circumference | true | Inferred relationship | Some | 6 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Has interpretation | Below reference range | true | Inferred relationship | Some | 6 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Finding site | Face structure | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Finding site | Cerebellar structure | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Finding site | Pontine structure | true | Inferred relationship | Some | 3 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 3 | |
Congenital pontocerebellar hypoplasia type 11 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)