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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

OMIM:611820

Subsets

DO_rare_slim

Synonyms

LQT11 [EXACT]

Parent Relationships

is_a long QT syndrome

is_a autosomal dominant disease

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