OBO ID: DOID:0111182 |
Term Name: | familial hemiplegic migraine 2 | Search Ontology: | |
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Definition: | A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in ATP1A2 on 1q23.2. https://www.ncbi.nlm.nih.gov/pubmed/12539047 | ||
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Ontology: | Human Disease ( DOID:0111182 ) |
OTHER familial hemiplegic migraine 2 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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