| familiaire hemiplegische migraine type 2 (aandoening) | | familiaire hemiplegische migraine type 2 | | Familial hemiplegic migraine type 2 | | Migraine type caused by mutations in the ATP1A2 gene. |
| | Id | 1260330000 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | G43.3 | | Rule | TRUE | | Advice | ALWAYS G43.3 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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