ZFIN Human Disease: long QT syndrome 12

OBO ID: DOID:0110653

OBO ID: DOID:0110653

Term Name:	long QT syndrome 12	Search Ontology:
Synonyms:	LQT12
Definition:	A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SNTA1 gene on chromosome 20q11.21. https://www.ncbi.nlm.nih.gov/pubmed/19684871
References:	ICD10CM:I45.8 MESH:C567842 OMIM:612955
Ontology:	Human Disease ( DOID:0110653 )

Relationships

is a type of:	autosomal dominant disease long QT syndrome autosomal dominant disease long QT syndrome Show first 5 Terms

OTHER long QT syndrome 12 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SNTA1	snta1	Long QT syndrome 12	612955

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None