catecholaminergic polymorphic ventricular tachycardia 5

Summary

DOID:0060679 - catecholaminergic polymorphic ventricular tachycardia 5

Disease Ontology Definition:A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal recessive inheritance and has_material_basis_in homozygous or compound heterozygous mutation in the TRDN gene on chromosome 6q22.

Synonyms: CVPT5

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

: trdn

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014191 - catecholaminergic polymorphic ventricular tachycardia 5

MONDO:0014191 - catecholaminergic polymorphic ventricular tachycardia 5

MIM:

MIM:615441 - CARDIAC ARRHYTHMIA SYNDROME, WITH OR WITHOUT SKELETAL MUSCLE WEAKNESS; CARDAR

MIM:615441 - CARDIAC ARRHYTHMIA SYNDROME, WITH OR WITHOUT SKELETAL MUSCLE WEAKNESS; CARDAR

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): catecholaminergic polymorphic ventricular tachycardia (is_a)