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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 MIM:603830
Subsets	DO_rare_slim
Synonyms	LQT3 [EXACT]
Parent Relationships	is_a long QT syndrome is_a digenic disease is_a autosomal dominant disease