Brugada syndrome 8

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Summary

Literature (0)

DOID:0110225 - Brugada syndrome 8

Disease Ontology Definition:A Brugada syndrome that has_material_basis_in heterozygous mutation in the HCN4 gene on chromosome 15q24.

Synonyms: BRGDA8

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

:

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013148 - early midbrain vesicle

MONDO:0013148 - early midbrain vesicle

MIM:

MIM:613123 - BRUGADA SYNDROME 8; BRGDA8

MIM:613123 - BRUGADA SYNDROME 8; BRGDA8

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)