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| Term | familial hemiplegic migraine 3 | ID (Ontology) | DOID:0111183 (Human Disease) |
| Definition | A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in SCN1A on 2q24.3. | ||
| Also Known As | "FHM3" ; "MHP3" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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migraine with aura |__familial hemiplegic migraine |__familial hemiplegic migraine 3 1 rec. |
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| Is a | familial hemiplegic migraine | ||
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External Crossreferences & Linkouts
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GARD:10974 MIM:609634 |
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