tricuspid valve stenosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A tricuspid valve disease that is characterized by the narrowing of the orifice of the tricuspid valve of the heart. This causes increased resistance to blood flow through the valve. (Human Disease Ontology, DOID_4078)
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2 gene mutations causing the tricuspid valve stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CNTRL centriolin
HEY2 hes-related family bHLH transcription factor with YRPW motif 2