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Metadata
ID	DOID:0110651
Name	long QT syndrome 10
Definition	A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3. https://www.ncbi.nlm.nih.gov/pubmed/17592081
Xrefs	GARD:10436 ICD10CM:I45.8 MESH:C567514 MIM:611819
Subsets	DO_rare_slim
Synonyms	LQT10 [EXACT]
Parent Relationships	is_a long QT syndrome is_a autosomal dominant disease