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Metadata
ID	DOID:0110652
Name	long QT syndrome 11
Definition	A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the AKAP9 gene on chromosome 7q21.2. https://www.ncbi.nlm.nih.gov/pubmed/18093912
Xrefs	GARD:10437 ICD10CM:I45.8 MESH:C567513 MIM:611820
Subsets	DO_rare_slim
Synonyms	LQT11 [EXACT]
Parent Relationships	is_a long QT syndrome is_a autosomal dominant disease
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance