GenTIGSA Gene Database on Rare Genetic Disorders
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Jervell And Lange-Nielsen Syndrome  
Disease Aliases (32)

Cardioauditory syndrome of jervell and lange-nielsen

Cardio auditory syncope syndrome

Cardio-auditory-syncope syndrome

Cardio-auditory-syncope syndromes

Cardio-auditory syndrome

Cardioauditory syndrome of jervell and lange nielsen

Deafness, congenital, and functional heart disease

Jlns

Jlns1

Jervell and lange nielsen syndrome 1

Jervell and lange-nielsen syndrome 1

Jervell lange nielsen syndrome

Jervell lange-nielsen syndrome

Jervell and lange nielsen syndrome

Jervell and lange-nielsen syndrome

Jervell and lange-nielsen syndrome 1; jlns1

Jervell and lange-nielsen syndrome caused by mutation in kcnq1

Jervell and lange-nielsen syndrome type 1

Jervell and lange-nielson syndrome

Jervell-lange nielsen syndrome

Kcnq1 jervell and lange-nielsen syndrome

Long qt interval - deafness

Long qt interval-deafness syndrome

Long qt interval-hearing loss syndrome

Prolonged qt interval in ekg and sudden death

Surdo-cardiac syndrome

Surdo cardiac syndrome

Surdo-cardiac syndromes

Syndrome, cardio-auditory-syncope

Syndrome, jervell-lange nielsen

Syndrome, surdo-cardiac

Syndromes, cardio-auditory-syncope

Associated Genes (2)
 

NCBI-RefSeq:  KCNE1   (Potassium voltage-gated channel subfamily E regulatory subunit 1)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  KCNQ1   (Potassium voltage-gated channel subfamily Q member 1)

External Links:  gnomAD browser   Ensembl   GeneCards

 


Cross-references of Jervell and Lange-Nielsen syndrome OMIM GARD Orphanet NCBI-GTR NCBI-MedGen MalaCards      MeSH Annotations