ZFIN Human Disease: long QT syndrome 9

OBO ID: DOID:0110650

OBO ID: DOID:0110650

Term Name:	long QT syndrome 9	Search Ontology:
Synonyms:	LQT9
Definition:	A long QT syndrome that has_material_basis_in mutation of the CAV3 gene on chromosome 3p25.3. https://www.ncbi.nlm.nih.gov/pubmed/17060380
References:	GARD:10435 ICD10CM:I45.8 MESH:C567515 OMIM:611818
Ontology:	Human Disease ( DOID:0110650 )

Relationships

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

OTHER long QT syndrome 9 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CAV3	cav3	Long QT syndrome 9	611818

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None