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DO Term : familial hemiplegic migraine 2 [DOID:0111182] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in ATP1A2 on 1q23.2.
  • synonyms:
  • GARD:10095,
  • OMIM:602481,
  • MHP2,
  • FHM2,
  • 602481,
  • Familial hemiplegic migraine-2
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Disease

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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