Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
105804012 | Disorder of manganese metabolism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
802963016 | Disorder of manganese metabolism (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4598271000241110 | trouble du métabolisme du manganèse | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Disorder of manganese metabolism | Is a | Disorder of trace mineral metabolism | true | Inferred relationship | Some | ||
Disorder of manganese metabolism | Finding site | Body system structure | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Manganese deficiency | Is a | False | Disorder of manganese metabolism | Inferred relationship | Some | |
Hypermanganesemia with dystonia, polycythaemia, and cirrhosis | Is a | False | Disorder of manganese metabolism | Inferred relationship | Some | |
An inherited disorder characterised by hypermanganesemia. Manganese accumulates in the region of the brain responsible for the coordination of movement causing dystonia and other uncontrolled movements. Two types of hypermanganesemia with dystonia have been identified; hypermanganesemia with dystonia, polycythaemia, and cirrhosis (HMDPC) and hypermanganesemia with dystonia 2 and they are distinguished by genetic cause and features. Inherited in an autosomal recessive pattern. | Is a | True | Disorder of manganese metabolism | Inferred relationship | Some |
This concept is not in any reference sets