Jervell and Lange-Nielsen syndrome
https://rarediseases.info.nih.gov/diseases/3048/jervell-lange-nielsen-syndrome
Jervell and Lange-Nielsen syndrome type 1
prolonged QT interval in EKG and sudden death
Jervell and Lange Nielsen syndrome
MONDO:0002441
Jervell Lange-Nielsen syndrome
MedDRA:10057936
DOID:2842
NORD:1310
OMIMPS:220400
An autosomal recessive inherited syndrome caused by mutations in the KCNE1 and KCNQ1 genes. It is characterized by congenital hearing loss and arrhythmia. It is a form of long QT syndrome.
SCTID:373905003
GARD:3048
Jervell-Lange Nielsen syndrome
Surdo-cardiac syndrome
deafness, congenital, and functional heart disease
NCIT:C84793
UMLS:C0022387
Jervell and Lange-Nielson syndrome
Cardioauditory syndrome of Jervell and Lange-Nielsen
JLNS1
Jervell and Lange-Nielsen syndrome 1
Orphanet:90647
MESH:D029593
long QT interval-deafness syndrome
familial long QT syndrome