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DO Term : familial hemiplegic migraine 1 [DOID:0111181] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A familial hemiplegic migraine that is commonly associated with cerebellar degeneration and has_material_basis_in heterozygous mutation in CACNA1A on 19p13.
  • synonyms:
  • OMIM:141500,
  • FHM1,
  • familial hemiplegic migraine1 with progressive cerebellar ataxia,
  • MHP1,
  • GARD:2638,
  • 141500
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Disease

Diseases --> Human genes

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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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