Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Dec 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5159126016 | PADDAS syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5159127013 | SCA47 - spinocerebellar ataxia type 47 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5159128015 | Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5159129011 | Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5159130018 | PUM1-associated developmental disability, ataxia, seizure syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Is a | Intellectual disability | true | Inferred relationship | Some | ||
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Is a | Spinocerebellar ataxia | true | Inferred relationship | Some | ||
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Is a | Developmental delay | true | Inferred relationship | Some | ||
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 5 | |
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Interprets | Intellectual ability (observable entity) | true | Inferred relationship | Some | 3 | |
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 3 | |
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Interprets | Adaptation behavior (observable entity) | true | Inferred relationship | Some | 4 | |
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 4 | |
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Finding site | Cerebellar structure | true | Inferred relationship | Some | 1 | |
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Finding site | Spinal cord structure | true | Inferred relationship | Some | 2 | |
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets