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Metadata
ID	DOID:0110653
Name	long QT syndrome 12
Definition	A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SNTA1 gene on chromosome 20q11.21. https://www.ncbi.nlm.nih.gov/pubmed/19684871
Xrefs	ICD10CM:I45.8 MESH:C567842 MIM:612955
Synonyms	LQT12 [EXACT]
Parent Relationships	is_a long QT syndrome is_a autosomal dominant disease
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance