Visualize Submit Comment
Metadata
ID DOID:0110648
Name long QT syndrome 6
Definition A long QT interval syndrome that has_material_basis_in dominant inheritance of mutation in the KCNE2 gene on chromosome 21q22.11.
https://www.ncbi.nlm.nih.gov/pubmed/10219239
Xrefs

GARD:10434

ICD10CM:I45.8

MESH:C566333

MIM:613693

Subsets

DO_rare_slim

Synonyms

LQT6 [EXACT]

Parent Relationships

is_a long QT syndrome

is_a autosomal dominant disease

is_a digenic disease

Subclass Logical Relationships

has material basis in some digenic inheritance

has material basis in some autosomal dominant inheritance

Add an item to the term tracker