Visualize Submit Comment
Metadata
ID DOID:0110646
Name long QT syndrome 3
Definition A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2.
https://www.ncbi.nlm.nih.gov/pubmed/8541846
Xrefs

GARD:3286

ICD10CM:I45.8

MESH:C565840

OMIM:603830

Subsets

DO_rare_slim

Synonyms

LQT3 [EXACT]

Parent Relationships

is_a long QT syndrome

is_a digenic disease

is_a autosomal dominant disease

Add an item to the term tracker