WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:0050451
Child Term . Identifier  DOID:0110221 Direct  true
Redundant  false
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1 Child Term

Identifier Name Description
DOID:0110221 Brugada syndrome 4 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.

1 Parent Term

Identifier Name Description
DOID:0050451 Brugada syndrome A heart conduction disease that is characterized by abnormal electrocardiogram (ECG) findings and an increased risk of sudden cardiac death.