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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 OMIM:613695
Subsets	DO_rare_slim
Synonyms	LQT5 [EXACT]
Parent Relationships	is_a long QT syndrome is_a digenic disease is_a autosomal dominant disease