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Metadata
ID	DOID:0110645
Name	long QT syndrome 2
Definition	A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1. https://www.ncbi.nlm.nih.gov/pubmed/7889573
Xrefs	GARD:3285 ICD10CM:I45.8 MESH:C563614 OMIM:613688
Subsets	DO_rare_slim
Synonyms	LQT2 [EXACT]
Parent Relationships	is_a long QT syndrome is_a digenic disease is_a autosomal dominant disease