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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

OMIM:611819

Subsets

DO_rare_slim

Synonyms

LQT10 [EXACT]

Parent Relationships

is_a long QT syndrome

is_a autosomal dominant disease

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