Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/611819 http://purl.bioontology.org/ontology/OMIM/611819
Preferred Name	LONG QT SYNDROME 10
Synonyms	LQT10 ATFB17 ATRIAL FIBRILLATION, FAMILIAL, 17
Type	http://www.w3.org/2002/07/owl#Class

altLabel	LQT10 ATFB17 ATRIAL FIBRILLATION, FAMILIAL, 17
prefLabel	LONG QT SYNDROME 10
Gene Symbol	SCN4B ATFB17 LQT10
Scope Statement	Caused by mutation in the type IV voltage-gated sodium channel beta subunit gene (SCN4B, 608256.0001) [MOLECULAR BASIS] Risk of sudden death with exertion [MISCELLANEOUS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU006249 http://purl.bioontology.org/ontology/OMIM/MTHU068866 http://purl.bioontology.org/ontology/OMIM/MTHU068864 http://purl.bioontology.org/ontology/OMIM/MTHU068865 http://purl.bioontology.org/ontology/OMIM/MTHU057326
tui	T047 T033
Gene Locus	11q23
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	611819
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047 http://purl.bioontology.org/ontology/STY/T033
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000018
cui	C2678484 C4013560
OMIM Entry Type	3
OMIM MimType Value	pound

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