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DOID:0110220 - Brugada syndrome 3
Disease Ontology Definition:A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the alpha-1C subunit of the L-type voltage-dependent calcium channel (CACNA1C) on chromosome 12p13.
Synonyms: BRGDA3,
Xenbase Genes : cacna1c
MONDO:0012742 - Brugada syndrome 3 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Brugada syndrome (is_a)