GlyCosmos Portal

Submissions

long QT syndrome

Summary

Synonym

LQT
long Q-T syndrome

Definition

An autosomal genetic disease that is characterized by delayed repolarization of the heart following a heartbeat increases the risk of episodes of torsade de pointes (TDP, a form of irregular heartbeat that originates from the ventricles).

Super Class

intrinsic cardiomyopathy

External Links

Disease Ontology

DOID:2843

Mondo Disease Ontology

MONDO:0002442

MeSH

D008133

UMLS

C0023976

NCI Thesaurus

C34786

ORDO

768

OMIM

PS192500

GARD

6922

Related Genes

Displaying entry **11 - 11** of 11 in total

« First

‹ Prev

1

2
Gene ID	Gene Symbol	Description	Source
144245	ALG10B	ALG10 alpha-1,2-glucosyltransferase B	DisGeNET

Displaying 1 entry
Gene ID	Gene Symbol	Description	Source
16535	Kcnq1	potassium voltage-gated channel, subfamily Q, member 1	Alliance of Genome Resources

Displaying 1 entry
Gene ID	Gene Symbol	Description	Source
84020	Kcnq1	potassium voltage-gated channel subfamily Q member 1	Alliance of Genome Resources

Related Glycoprotein

Displaying **all 8** entries
UniProt ID	Protein Name	Source
O00767	Stearoyl-CoA desaturase	DisGeNET DisGeNET DisGeNET
P04798	Cytochrome P450 1A1	DisGeNET
P11310	Medium-chain specific acyl-CoA dehydrogenase, mitochondrial	DisGeNET
P22732	Solute carrier family 2, facilitated glucose transporter member 5	DisGeNET
P60484	Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN	DisGeNET
Q5BKT4	Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase	DisGeNET
Q5I7T1	Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase	DisGeNET
Q9P232	Contactin-3	DisGeNET