| 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. |
| | Id | 768553002 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | E88.8 | | Rule | TRUE | | Advice | ALWAYS E88.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
| Target | G24.9 | | Rule | TRUE | | Advice | ALWAYS G24.9 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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