Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3321085018 | Arterial dissection and lentiginosis syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3321086017 | Arterial dissection and lentiginosis syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5402377011 | A rare association syndrome, reported in several members of two families to date, characterized by arterial dissection, occurring at an early age and presenting with a range of manifestations depending on the vascular territory involved (headache, dysphasia, hemiparesis), in association with cystic medial necrosis and multiple lentigines (brown and black in color and mainly affecting the skin of the trunk and extremities). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402378018 | A rare association syndrome, reported in several members of two families to date, characterised by arterial dissection, occurring at an early age and presenting with a range of manifestations depending on the vascular territory involved (headache, dysphasia, hemiparesis), in association with cystic medial necrosis and multiple lentigines (brown and black in colour and mainly affecting the skin of the trunk and extremities). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Arterial dissection and lentiginosis syndrome (disorder) | Associated morphology | Increased melanin pigmentation | false | Inferred relationship | Some | 5 | |
Arterial dissection and lentiginosis syndrome (disorder) | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
Arterial dissection and lentiginosis syndrome (disorder) | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
Arterial dissection and lentiginosis syndrome (disorder) | Is a | Hereditary lentiginosis | false | Inferred relationship | Some | ||
Arterial dissection and lentiginosis syndrome (disorder) | Is a | Dissection of artery | true | Inferred relationship | Some | ||
Arterial dissection and lentiginosis syndrome (disorder) | Associated morphology | Dissecting hemorrhage | false | Inferred relationship | Some | 3 | |
Arterial dissection and lentiginosis syndrome (disorder) | Finding site | Wall of artery | false | Inferred relationship | Some | 3 | |
Arterial dissection and lentiginosis syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 4 | |
Arterial dissection and lentiginosis syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 5 | |
Arterial dissection and lentiginosis syndrome (disorder) | Associated morphology | Melanosis | false | Inferred relationship | Some | 4 | |
Arterial dissection and lentiginosis syndrome (disorder) | Is a | Genetic disorder of skin pigmentation (disorder) | false | Inferred relationship | Some | ||
Arterial dissection and lentiginosis syndrome (disorder) | Associated morphology | Lentigo (morphologic abnormality) | false | Inferred relationship | Some | 2 | |
Arterial dissection and lentiginosis syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Arterial dissection and lentiginosis syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Arterial dissection and lentiginosis syndrome (disorder) | Is a | Familial generalised lentiginosis | false | Inferred relationship | Some | ||
Arterial dissection and lentiginosis syndrome (disorder) | Is a | Arterial malformation | true | Inferred relationship | Some | ||
Arterial dissection and lentiginosis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | false | Inferred relationship | Some | 1 | |
Arterial dissection and lentiginosis syndrome (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
Arterial dissection and lentiginosis syndrome (disorder) | Associated morphology | Dissecting hemorrhage | true | Inferred relationship | Some | 2 | |
Arterial dissection and lentiginosis syndrome (disorder) | Associated morphology | Lentigo (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
Arterial dissection and lentiginosis syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Arterial dissection and lentiginosis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Arterial dissection and lentiginosis syndrome (disorder) | Finding site | Wall of artery | true | Inferred relationship | Some | 2 | |
Arterial dissection and lentiginosis syndrome (disorder) | Is a | Congenital melanosis | true | Inferred relationship | Some | ||
Arterial dissection and lentiginosis syndrome (disorder) | Is a | Congenital hamartoma of skin (disorder) | true | Inferred relationship | Some | ||
Arterial dissection and lentiginosis syndrome (disorder) | Is a | Lentiginosis (disorder) | true | Inferred relationship | Some | ||
Arterial dissection and lentiginosis syndrome (disorder) | Is a | Congenital pigmentary skin anomalies | false | Inferred relationship | Some | ||
Arterial dissection and lentiginosis syndrome (disorder) | Is a | Hereditary hypermelanosis (disorder) | true | Inferred relationship | Some | ||
Arterial dissection and lentiginosis syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)