| | syndroom van vroeg optredende neurodegeneratie, choreatische bewegingen en microcytaire anemie door mutatie in 'iron responsive element binding protein 2'-gen (aandoening) |  |  | syndroom van vroeg optredende neurodegeneratie, choreatische bewegingen en microcytaire anemie door mutatie in 'iron responsive element binding protein 2'-gen |  |  | syndroom van vroeg optredende neurodegeneratie, choreatische bewegingen en microcytaire anemie door mutatie in IREB2-genNDCAMA
 
 |  |  | Early-onset neurodegeneration, choreoathetoid movement, microcytic anemia due to IREB2 mutation |  |  | NDCAMA - neurodegeneration, choreoathetoid movement, microcytic anemiaEarly-onset neurodegeneration, choreoathetoid movement, microcytic anemia due to iron responsive element binding protein 2 gene mutation
 
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 | | Id | 1366590005 |  | Status | Primitive | 
| SNOMED CT to ICD-10 extended map |  | | Target | G31.8 |  | Rule | TRUE |  | Advice | ALWAYS G31.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION |  | Correlation | SNOMED CT source code to target map code correlation not specified | 
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