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DO Term : Brugada syndrome 4 [DOID:0110221] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the beta-2 subunit of the voltage-dependent L-type calcium channel (CACNB2) on chromosome 10p12.
  • synonyms:
  • 611876,
  • ICD10CM:I49.8,
  • OMIM:611876,
  • GARD:10362,
  • BRGDA4,
  • MESH:C567508
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Disease

Diseases --> Human genes

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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents





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