Status: current, Primitive. Date: 31-Dec 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5159126016 | PADDAS syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
5159127013 | SCA47 - spinocerebellar ataxia type 47 | en | Synonym | Active | Case sensitive | SNOMED CT core |
5159128015 | Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
5159129011 | Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
5159130018 | PUM1-associated developmental disability, ataxia, seizure syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
5159140015 | A rare genetic syndromic intellectual disability characterised by developmental delay, intellectual disability, ataxia, and more variably seizures and short stature. Behavioural abnormalities may also be observed, along with variable facial and other dysmorphic features (such as broad nasal bridge, hypertelorism, almond-shaped eyes, high-arched palate and anomalies of the fingers and toes). Brain imaging may reveal dilated ventricles, small corpus callosum or posterior fossa abnormalities. | en | Definition | Active | Case sensitive | SNOMED CT core |
5159141016 | A rare genetic syndromic intellectual disability characterized by developmental delay, intellectual disability, ataxia, and more variably seizures and short stature. Behavioral abnormalities may also be observed, along with variable facial and other dysmorphic features (such as broad nasal bridge, hypertelorism, almond-shaped eyes, high-arched palate and anomalies of the fingers and toes). Brain imaging may reveal dilated ventricles, small corpus callosum or posterior fossa abnormalities. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
PUM1-associated developmental disability, ataxia, seizure syndrome | Is a | Intellectual disability | true | Inferred relationship | Some | ||
PUM1-associated developmental disability, ataxia, seizure syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
PUM1-associated developmental disability, ataxia, seizure syndrome | Is a | Spinocerebellar ataxia | true | Inferred relationship | Some | ||
PUM1-associated developmental disability, ataxia, seizure syndrome | Is a | Developmental delay | true | Inferred relationship | Some | ||
PUM1-associated developmental disability, ataxia, seizure syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
PUM1-associated developmental disability, ataxia, seizure syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 5 | |
PUM1-associated developmental disability, ataxia, seizure syndrome | Interprets | Intellectual ability | true | Inferred relationship | Some | 3 | |
PUM1-associated developmental disability, ataxia, seizure syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 3 | |
PUM1-associated developmental disability, ataxia, seizure syndrome | Interprets | Adaptation behaviour | true | Inferred relationship | Some | 4 | |
PUM1-associated developmental disability, ataxia, seizure syndrome | Has interpretation | Impaired | true | Inferred relationship | Some | 4 | |
PUM1-associated developmental disability, ataxia, seizure syndrome | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
PUM1-associated developmental disability, ataxia, seizure syndrome | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
PUM1-associated developmental disability, ataxia, seizure syndrome | Finding site | Spinal cord structure | true | Inferred relationship | Some | 2 | |
PUM1-associated developmental disability, ataxia, seizure syndrome | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set