Brugada syndrome 5

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Summary

Literature (0)

DOID:0110222 - Brugada syndrome 5

Disease Ontology Definition:A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN1B gene on chromosome 19q13.

Synonyms: BRGDA5

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: scn1b

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013015 - Brugada syndrome 5

MONDO:0013015 - Brugada syndrome 5

MIM:

MIM:612838 - BRUGADA SYNDROME 5; BRGDA5

MIM:612838 - BRUGADA SYNDROME 5; BRGDA5

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)