Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4639180016 | Pontine autosomal dominant microangiopathy with leukoencephalopathy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4639181017 | Pontine autosomal dominant microangiopathy with leukoencephalopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
4639182012 | Pontine autosomal dominant microangiopathy with leucoencephalopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
4639183019 | PADMAL - pontine autosomal dominant microangiopathy with leukoencephalopathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
4639184013 | PADMAL - pontine autosomal dominant microangiopathy with leucoencephalopathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
4639185014 | A rare genetic cerebral small vessel disease characterized by recurrent ischemic strokes, often with a predilection for the pons, with typical onset in the fourth or fifth decade of life. Patients present progressive cognitive and motor impairment with pyramidal, bulbar and cerebellar symptoms among others. Brain imaging shows multiple lacunar infarcts, typically with involvement of the pons, as well as variable leukoencephalopathy of the cerebral hemispheres. | en | Definition | Active | Case sensitive | SNOMED CT core |
4639186010 | A rare genetic cerebral small vessel disease characterised by recurrent ischaemic strokes, often with a predilection for the pons, with typical onset in the fourth or fifth decade of life. Patients present progressive cognitive and motor impairment with pyramidal, bulbar and cerebellar symptoms among others. Brain imaging shows multiple lacunar infarcts, typically with involvement of the pons, as well as variable leucoencephalopathy of the cerebral hemispheres. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Pontine autosomal dominant microangiopathy with leucoencephalopathy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Pontine autosomal dominant microangiopathy with leucoencephalopathy | Is a | Chronic disease of cardiovascular system | true | Inferred relationship | Some | ||
Pontine autosomal dominant microangiopathy with leucoencephalopathy | Is a | Leukoencephalopathy | true | Inferred relationship | Some | ||
Pontine autosomal dominant microangiopathy with leucoencephalopathy | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
Pontine autosomal dominant microangiopathy with leucoencephalopathy | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Pontine autosomal dominant microangiopathy with leucoencephalopathy | Is a | Small vessel cerebrovascular disease | true | Inferred relationship | Some | ||
Pontine autosomal dominant microangiopathy with leucoencephalopathy | Is a | Chronic brain syndrome | true | Inferred relationship | Some | ||
Pontine autosomal dominant microangiopathy with leucoencephalopathy | Clinical course | Progressive | true | Inferred relationship | Some | 1 | |
Pontine autosomal dominant microangiopathy with leucoencephalopathy | Finding site | Cerebrovascular system structure | true | Inferred relationship | Some | 2 | |
Pontine autosomal dominant microangiopathy with leucoencephalopathy | Finding site | Cerebral white matter structure | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set