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Metadata
ID DOID:0110647
Name long QT syndrome 5
Definition A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNE1 gene on chromosome 21q22.12.
https://www.ncbi.nlm.nih.gov/pubmed/10973849
Xrefs

GARD:10433

ICD10CM:I45.8

MESH:C566766

MIM:613695

Subsets

DO_rare_slim

Synonyms

LQT5 [EXACT]

Parent Relationships

is_a long QT syndrome

is_a digenic disease

is_a autosomal dominant disease

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