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hypermanganesemie met dystonie (aandoening)
hypermanganesemie met dystonie
Hypermanganesemia with dystonia
HMNDYT - hypermanganesemia with dystonia
Familial manganese-induced neurotoxicity
An inherited disorder characterized 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, polycythemia, and cirrhosis (HMDPC) and hypermanganesemia with dystonia 2 and they are distinguished by genetic cause and features. Inherited in an autosomal recessive pattern.
Id768553002
StatusPrimitive
referentieset met complexe 'mapping' naar ICD-10
TargetE88.8
RuleTRUE
AdviceALWAYS E88.8
CorrelationSNOMED CT source code to target map code correlation not specified
TargetG24.9
RuleTRUE
AdviceALWAYS G24.9
CorrelationSNOMED CT source code to target map code correlation not specified
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